Variant report

Variant	rs6993706
Chromosome Location	chr8:1718389-1718390
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	chr8:1717127-1718675	K562	blood:	n/a	n/a
2	POLR2A	chr8:1716444-1720073	HepG2	liver:	n/a	n/a
3	POLR2A	chr8:1718377-1719199	A549	lung:	n/a	n/a
4	POLR2A	chr8:1716558-1718983	PBDE	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1715604..1719309-chr8:1719775..1722697,3	MCF-7	breast:
2	chr8:1716952..1719420-chr8:1723630..1725290,2	K562	blood:
3	chr8:1717537..1720996-chr8:1730538..1734244,3	K562	blood:
4	chr8:1716779..1719807-chr8:1720104..1723417,3	K562	blood:

Variant related genes	Relation type
CLN8	TF binding region
ENSG00000182372	Chromatin interaction

Extended variants
information (count: 121 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10087654	0.91[ASN][1000 genomes]
rs10089222	0.85[ASN][1000 genomes]
rs10097891	0.94[CHB][hapmap];0.94[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs10100341	0.94[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs10102731	0.91[ASN][1000 genomes]
rs10105317	0.81[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs10106153	0.87[ASN][1000 genomes]
rs10113471	0.82[ASN][1000 genomes]
rs10481354	0.81[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11136421	0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs11136422	0.83[ASN][1000 genomes]
rs11136424	0.94[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11778824	1.00[CHB][hapmap];0.91[CHD][hapmap];0.89[JPT][hapmap];0.82[MEX][hapmap];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11986414	0.82[MEX][hapmap];0.81[AMR][1000 genomes]
rs12335115	0.85[ASN][1000 genomes]
rs12674711	0.84[ASN][1000 genomes]
rs13251071	0.81[ASN][1000 genomes]
rs13256424	0.92[ASN][1000 genomes]
rs13261755	0.82[ASN][1000 genomes]
rs13282161	0.84[ASN][1000 genomes]
rs13540	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2293977	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28376731	0.86[ASN][1000 genomes]
rs2957085	0.87[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs35062922	0.82[ASN][1000 genomes]
rs3812477	0.87[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4242538	0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs4242539	0.94[JPT][hapmap]
rs4370560	0.88[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4372027	0.92[ASN][1000 genomes]
rs4595147	0.81[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4639549	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4875806	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4875889	0.82[ASN][1000 genomes]
rs4875957	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4875958	0.94[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6558518	0.85[ASN][1000 genomes]
rs6558520	0.81[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs6558521	0.81[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs6558522	0.81[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs6558523	0.81[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs6558524	0.87[ASN][1000 genomes]
rs6558525	0.81[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs6558526	0.85[ASN][1000 genomes]
rs6558527	0.87[CHB][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6558528	0.84[ASN][1000 genomes]
rs6558530	0.82[ASN][1000 genomes]
rs6558531	0.92[ASN][1000 genomes]
rs6558532	0.90[ASN][1000 genomes]
rs6558533	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6558534	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6558535	0.92[ASN][1000 genomes]
rs6558536	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6558538	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6981804	0.87[ASN][1000 genomes]
rs6982516	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6984632	0.84[ASN][1000 genomes]
rs6986102	0.80[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6991773	0.93[ASN][1000 genomes]
rs6991783	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7000162	0.95[ASN][1000 genomes]
rs7001282	0.87[ASN][1000 genomes]
rs7005592	0.87[CHB][hapmap];0.88[CHD][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];0.87[ASN][1000 genomes]
rs7005699	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs7008465	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7010616	0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7013835	0.83[ASN][1000 genomes]
rs7013841	0.83[ASN][1000 genomes]
rs7014327	0.94[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs7014823	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7015858	0.94[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs71499040	0.91[ASN][1000 genomes]
rs730377	0.92[ASN][1000 genomes]
rs730379	0.91[ASN][1000 genomes]
rs7341635	0.92[ASN][1000 genomes]
rs7459507	0.84[ASN][1000 genomes]
rs7460230	0.84[ASN][1000 genomes]
rs7460287	0.87[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7460365	0.86[ASN][1000 genomes]
rs7460866	0.86[ASN][1000 genomes]
rs7460972	0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7461159	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7461259	0.82[ASN][1000 genomes]
rs7461600	0.92[ASN][1000 genomes]
rs7462693	0.80[AMR][1000 genomes]
rs7463876	0.91[ASN][1000 genomes]
rs7463879	0.89[ASN][1000 genomes]
rs7465178	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7818406	0.80[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs7822816	0.89[ASN][1000 genomes]
rs7827009	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7827285	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7828950	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7838456	0.92[ASN][1000 genomes]
rs7842425	0.81[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7844748	0.81[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs7845723	0.81[CHB][hapmap];0.91[CHD][hapmap];0.89[JPT][hapmap]
rs7846610	0.81[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9022	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs6993706	CTD-2336O2.1	cis	Muscle Skeletal	GTEx
rs6993706	CTD-2336O2.1	cis	Adipose Subcutaneous	GTEx
rs6993706	CTD-2336O2.1	cis	Artery Tibial	GTEx
rs6993706	CTD-2336O2.1	cis	Thyroid	GTEx
rs6993706	CTD-2336O2.1	cis	lung	GTEx
rs6993706	CTD-2336O2.1	cis	Nerve Tibial	GTEx
rs6993706	CTD-2336O2.1	cis	Esophagus Muscularis	GTEx
rs6993706	CLN8	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1713000-1719200	Weak transcription	Ovary	ovary
2	chr8:1713400-1719600	Weak transcription	Colon Smooth Muscle	Colon
3	chr8:1713400-1721000	Weak transcription	Psoas Muscle	Psoas
4	chr8:1713400-1727000	Weak transcription	NHDF-Ad	bronchial
5	chr8:1713400-1735800	Weak transcription	Fetal Brain Male	brain
6	chr8:1713600-1719200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr8:1713600-1719200	Weak transcription	Brain Germinal Matrix	brain
8	chr8:1713600-1719200	Weak transcription	Fetal Brain Female	brain
9	chr8:1713600-1719400	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:1713600-1719400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:1713600-1719400	Weak transcription	Osteobl	bone
12	chr8:1713600-1721400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:1713600-1729600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr8:1713800-1718800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr8:1713800-1719200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr8:1714000-1718600	Enhancers	Left Ventricle	heart
17	chr8:1714000-1728000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr8:1714000-1729800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr8:1714400-1719000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr8:1714400-1729200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr8:1714800-1720000	Strong transcription	Primary T cells from cord blood	blood
22	chr8:1714800-1727000	Strong transcription	Fetal Intestine Small	intestine
23	chr8:1715200-1719600	Weak transcription	Dnd41	blood
24	chr8:1715400-1719200	Weak transcription	Thymus	Thymus
25	chr8:1715400-1726800	Strong transcription	Fetal Stomach	stomach
26	chr8:1715400-1727800	Weak transcription	Small Intestine	intestine
27	chr8:1715400-1729200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr8:1715600-1719000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr8:1715600-1719200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr8:1715600-1719200	Weak transcription	Fetal Thymus	thymus
31	chr8:1715600-1725600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr8:1716000-1718600	Enhancers	Spleen	Spleen
33	chr8:1716200-1719600	Weak transcription	GM12878-XiMat	blood
34	chr8:1716400-1718400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:1716400-1718600	Enhancers	Brain Cingulate Gyrus	brain
36	chr8:1716400-1718600	Enhancers	Brain Hippocampus Middle	brain
37	chr8:1716400-1726800	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr8:1716600-1718600	Enhancers	Brain Substantia Nigra	brain
39	chr8:1716600-1718600	Genic enhancers	Pancreas	Pancrea
40	chr8:1716600-1718600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
41	chr8:1716600-1719000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr8:1716600-1719800	Genic enhancers	Primary B cells from peripheral blood	blood
43	chr8:1716600-1723000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr8:1716600-1725200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr8:1716600-1727000	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr8:1716800-1718400	Enhancers	Placenta Amnion	Placenta Amnion
47	chr8:1716800-1718600	Genic enhancers	Lung	lung
48	chr8:1716800-1721000	Strong transcription	Liver	Liver
49	chr8:1716800-1721200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:1716800-1722000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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