Variant report

Variant	rs199530
Chromosome Location	chr17:44836653-44836654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:44836082..44838287-chr17:44847835..44850037,2	MCF-7	breast:
2	chr17:44833273..44837088-chr17:44837902..44840947,3	K562	blood:
3	chr17:44834549..44837328-chr17:44842622..44845050,2	K562	blood:

Extended variants
information (count: 111 )
Associated
traits (count: 86 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10491141	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12325819	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12452215	0.95[ASN][1000 genomes]
rs12603920	0.98[ASN][1000 genomes]
rs12937492	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12947457	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs142167	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs169201	0.94[CEU][hapmap]
rs16941674	0.99[ASN][1000 genomes]
rs17692129	0.89[JPT][hapmap]
rs183211	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199436	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199437	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs199438	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199439	0.89[CEU][hapmap]
rs199442	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs199443	0.89[CEU][hapmap]
rs199444	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs199445	0.89[CEU][hapmap]
rs199446	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs199448	0.89[CEU][hapmap]
rs199449	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs199451	0.89[CEU][hapmap]
rs199452	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199453	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199454	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199455	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs199456	0.89[CEU][hapmap]
rs199457	0.89[CEU][hapmap]
rs199498	0.86[GIH][hapmap]
rs199501	0.94[CEU][hapmap];1.00[GIH][hapmap];0.96[MEX][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.90[EUR][1000 genomes]
rs199505	0.83[CEU][hapmap]
rs199506	0.84[CEU][hapmap]
rs199507	0.82[CEU][hapmap]
rs199508	0.93[EUR][1000 genomes]
rs199509	0.84[CEU][hapmap]
rs199513	0.84[CEU][hapmap]
rs199514	0.84[CEU][hapmap]
rs199515	0.84[CEU][hapmap]
rs199516	0.84[CEU][hapmap]
rs199517	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs199518	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs199519	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199520	0.94[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.86[LWK][hapmap];0.92[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199521	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199523	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199524	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199526	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs199527	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs199528	0.84[CEU][hapmap]
rs199529	0.89[EUR][1000 genomes]
rs199531	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs199533	0.89[CEU][hapmap]
rs199534	0.89[CEU][hapmap]
rs199535	0.89[CEU][hapmap]
rs199536	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2316278	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs34565941	0.93[ASN][1000 genomes]
rs34720194	0.94[ASN][1000 genomes]
rs35937770	0.89[JPT][hapmap]
rs4141293	0.93[ASN][1000 genomes]
rs415430	0.84[CEU][hapmap]
rs4246416	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4968239	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs538628	0.89[CEU][hapmap]
rs62074082	0.85[ASN][1000 genomes]
rs6503809	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs67143796	0.93[ASN][1000 genomes]
rs67474242	0.94[ASN][1000 genomes]
rs70602	0.84[CEU][hapmap]
rs7216231	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[ASN][1000 genomes]
rs7224296	0.85[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7226263	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[ASN][1000 genomes]
rs72628337	0.93[ASN][1000 genomes]
rs72628338	0.86[ASN][1000 genomes]
rs757190	0.80[JPT][hapmap]
rs8065602	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9896243	0.89[CEU][hapmap]
rs9902077	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9912530	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431716	chr17:43893020-44868187	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	62 gene(s)	inside rSNPs	diseases
2	nsv431718	chr17:44094463-44873614	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv431729	chr17:44144214-44869063	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv2757660	chr17:44162284-44868187	Enhancers Genic enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription 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	54 gene(s)	inside rSNPs	diseases
5	nsv431805	chr17:44165803-44868430	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	esv3492820	chr17:44174959-45161556	Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	esv3492821	chr17:44174959-45161556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv916432	chr17:44223908-44873614	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	esv1819056	chr17:44391822-44873614	Enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	esv1844763	chr17:44391822-44913631	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	nsv428343	chr17:44391822-44913631	Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
14	esv1806073	chr17:44443111-44873614	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
15	nsv531823	chr17:44485771-45067769	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	esv1850605	chr17:44537030-44913631	Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
17	esv1792649	chr17:44627136-44849634	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	esv1820936	chr17:44629166-44848916	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	esv1812673	chr17:44648058-44849188	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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 target site	15 gene(s)	inside rSNPs	diseases
20	esv1818423	chr17:44648058-44849634	Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
21	esv1805955	chr17:44654416-44849188	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS 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	15 gene(s)	inside rSNPs	diseases
22	esv1818944	chr17:44662268-44859144	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
23	esv1796587	chr17:44680207-44849634	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
24	esv1803101	chr17:44680207-44849634	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
25	esv1803756	chr17:44680207-44865439	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
26	nsv833465	chr17:44706496-44889749	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
27	esv1843460	chr17:44732200-44913631	Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
28	esv1810528	chr17:44814884-44849634	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
29	esv1845488	chr17:44816132-44849634	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
30	nsv908562	chr17:44828931-45102413	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
31	nsv949295	chr17:44836653-45080757	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:86)

SNP	Gene	Cis/trans	Tissue	Source
rs199530	NSF	cis	normal skin	skin_eQTL
rs199530	RP11-259G18.3	cis	Thyroid	GTEx
rs199530	LRRC37A2	cis	Artery Tibial	GTEx
rs199530	LRRC37A17P	cis	Esophagus Mucosa	GTEx
rs199530	RP11-259G18.3	cis	Esophagus Muscularis	GTEx
rs199530	LRRC37A	cis	Nerve Tibial	GTEx
rs199530	BRCA1	cis	parietal	SCAN
rs199530	LRRC37A	cis	Muscle Skeletal	GTEx
rs199530	KIAA1267	cis	lesional skin	skin_eQTL
rs199530	MAPK8IP1	cis	Cerebellum	GTEx
rs199530	HAP1	cis	cerebellum	SCAN
rs199530	LRRC37A	cis	Frontal Cortex	GTEx
rs199530	KANSL1-AS1	cis	Heart Left Ventricle	GTEx
rs199530	LRRC37A	cis	brain	seeQTL
rs199530	RP11-259G18.2	cis	Esophagus Mucosa	GTEx
rs199530	RP11-259G18.2	cis	Skin Sun Exposed Lower leg	GTEx
rs199530	KANSL1-AS1	cis	Esophagus Muscularis	GTEx
rs199530	LRRC37A	cis	Esophagus Muscularis	GTEx
rs199530	KRT19	cis	cerebellum	SCAN
rs199530	MAPT	cis	Cerebellum	GTEx
rs199530	LRRC37A	cis	Artery Aorta	GTEx
rs199530	LOC644246	cis	lesional skin	skin_eQTL
rs199530	RP11-259G18.3	cis	Esophagus Mucosa	GTEx
rs199530	KIAA1267	cis	uninvolved skin	skin_eQTL
rs199530	FLJ10120	cis	multi-tissue	Pritchard
rs199530	LOC201175	cis	multi-tissue	Pritchard
rs199530	RP11-259G18.2	cis	Muscle Skeletal	GTEx
rs199530	RP11-259G18.3	cis	Artery Aorta	GTEx
rs199530	LRRC37A2	cis	Nerve Tibial	GTEx
rs199530	RP11-259G18.3	cis	Stomach	GTEx
rs199530	RP11-259G18.3	cis	Adipose Subcutaneous	GTEx
rs199530	LRRC37A2	cis	lung	GTEx
rs199530	LRRC37A	cis	Artery Tibial	GTEx
rs199530	KANSL1-AS1	cis	Whole Blood	GTEx
rs199530	ARL17B	cis	lymphoblastoid	seeQTL
rs199530	KANSL1-AS1	cis	lung	GTEx
rs199530	LRRC37A	cis	lung	GTEx
rs199530	RP11-259G18.2	cis	Whole Blood	GTEx
rs199530	C17orf69	cis	multi-tissue	Pritchard
rs199530	LRRC37A2	cis	Esophagus Muscularis	GTEx
rs199530	KANSL1-AS1	cis	Nerve Tibial	GTEx
rs199530	FALZ	trans	multi-tissue	Pritchard
rs199530	RP11-259G18.2	cis	lung	GTEx
rs199530	RP11-259G18.3	cis	Whole Blood	GTEx
rs199530	RP11-259G18.2	cis	Artery Aorta	GTEx
rs199530	LRRC37A	cis	Thyroid	GTEx
rs199530	KIAA1267	cis	normal skin	skin_eQTL
rs199530	RP11-259G18.2	cis	Artery Tibial	GTEx
rs199530	LOC644246///LOC649063	cis	lesional skin	skin_eQTL
rs199530	GJC1	cis	parietal	SCAN
rs199530	RP11-259G18.3	cis	Artery Tibial	GTEx
rs199530	RP11-259G18.3	cis	Muscle Skeletal	GTEx
rs199530	RP11-259G18.3	cis	Nerve Tibial	GTEx
rs199530	LOC644246///LOC649063	cis	uninvolved skin	skin_eQTL
rs199530	RP11-259G18.2	cis	Stomach	GTEx
rs199530	WNT3	cis	Artery Aorta	GTEx
rs199530	RP11-259G18.2	cis	Heart Left Ventricle	GTEx
rs199530	KANSL1-AS1	cis	Skin Sun Exposed Lower leg	GTEx
rs199530	SLC25A39	cis	cerebellum	SCAN
rs199530	RP11-259G18.2	cis	Adipose Subcutaneous	GTEx
rs199530	MAPK8IP1	trans	multi-tissue	Pritchard
rs199530	RP11-259G18.3	cis	Heart Left Ventricle	GTEx
rs199530	LRRC37A2	cis	Adipose Subcutaneous	GTEx
rs199530	WNT3	cis	Thyroid	GTEx
rs199530	KANSL1-AS1	cis	Artery Aorta	GTEx
rs199530	LRRC37A	cis	Stomach	GTEx
rs199530	KANSL1-AS1	cis	Artery Tibial	GTEx
rs199530	LRRC37A	cis	Esophagus Mucosa	GTEx
rs199530	MGC57346	cis	multi-tissue	Pritchard
rs199530	LRRC37A2	cis	Artery Aorta	GTEx
rs199530	RP11-259G18.2	cis	Esophagus Muscularis	GTEx
rs199530	RP11-259G18.3	cis	Skin Sun Exposed Lower leg	GTEx
rs199530	LOC646043	trans	multi-tissue	Pritchard
rs199530	KANSL1-AS1	cis	Muscle Skeletal	GTEx
rs199530	KRT26	cis	cerebellum	SCAN
rs199530	RP11-259G18.3	cis	lung	GTEx
rs199530	RP11-259G18.2	cis	Thyroid	GTEx
rs199530	LRRC37A	cis	Adipose Subcutaneous	GTEx
rs199530	KANSL1-AS1	cis	Esophagus Mucosa	GTEx
rs199530	NSF	cis	multi-tissue	Pritchard
rs199530	LRRC37A2	cis	Muscle Skeletal	GTEx
rs199530	KANSL1-AS1	cis	Thyroid	GTEx
rs199530	KANSL1-AS1	cis	Adipose Subcutaneous	GTEx
rs199530	LRRC37A2	cis	Skin Sun Exposed Lower leg	GTEx
rs199530	RP11-259G18.2	cis	Nerve Tibial	GTEx
rs199530	FMNL1	cis	cerebellum	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44793600-44842200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr17:44798600-44841800	Weak transcription	Right Ventricle	heart
3	chr17:44814400-44839000	Weak transcription	Fetal Brain Female	brain
4	chr17:44818800-44842200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr17:44819200-44841400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr17:44820600-44844400	Weak transcription	Small Intestine	intestine
7	chr17:44820800-44840600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr17:44820800-44841800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:44821200-44841000	Weak transcription	NH-A	brain
10	chr17:44821200-44841800	Weak transcription	NHLF	lung
11	chr17:44822400-44837600	Strong transcription	Primary T cells from cord blood	blood
12	chr17:44823400-44837600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr17:44825200-44837400	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr17:44825600-44837200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr17:44825600-44837400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr17:44825600-44837600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr17:44826200-44841800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr17:44826600-44837400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr17:44826800-44837600	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr17:44827000-44837200	Strong transcription	Adipose Nuclei	Adipose
21	chr17:44828400-44847800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:44829600-44839600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr17:44829600-44844000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr17:44829800-44842000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr17:44829800-44848000	Weak transcription	Fetal Kidney	kidney
26	chr17:44830200-44841800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr17:44832400-44847800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr17:44833000-44840600	Weak transcription	HUVEC	blood vessel
29	chr17:44833600-44839400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr17:44833600-44841800	Weak transcription	Fetal Brain Male	brain
31	chr17:44833600-44842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr17:44833600-44842400	Weak transcription	Brain Anterior Caudate	brain
33	chr17:44833800-44836800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr17:44833800-44841400	Weak transcription	Brain Germinal Matrix	brain
35	chr17:44833800-44841800	Weak transcription	HMEC	breast
36	chr17:44834000-44842200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr17:44834000-44846800	Weak transcription	Ovary	ovary
38	chr17:44834200-44837600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr17:44834200-44841800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr17:44834400-44836800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr17:44834400-44841400	Weak transcription	Colonic Mucosa	Colon
42	chr17:44834400-44841400	Weak transcription	Lung	lung
43	chr17:44834400-44841800	Weak transcription	Fetal Lung	lung
44	chr17:44834400-44842000	Weak transcription	Psoas Muscle	Psoas
45	chr17:44834400-44842200	Weak transcription	Brain Substantia Nigra	brain
46	chr17:44834400-44846400	Strong transcription	Fetal Intestine Small	intestine
47	chr17:44834600-44836800	Weak transcription	Primary B cells from cord blood	blood
48	chr17:44834600-44837200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr17:44834600-44837600	Strong transcription	Primary B cells from peripheral blood	blood
50	chr17:44834600-44838400	Weak transcription	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links