Variant report

Variant	rs888669
Chromosome Location	chr19:18540644-18540645
allele	C/T
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	ZNF143	chr19:18540637-18540968	K562	blood:	n/a	n/a
2	POLR2A	chr19:18538913-18542153	SK-N-MC	brain:	n/a	n/a
3	ZBTB7A	chr19:18539505-18540853	ECC-1	luminal epithelium:	n/a	chr19:18540747-18540755
4	YY1	chr19:18539630-18540878	K562	blood:	n/a	chr19:18540470-18540479 chr19:18540151-18540165 chr19:18540055-18540064 chr19:18540275-18540284 chr19:18540052-18540061 chr19:18540276-18540287 chr19:18540278-18540287 chr19:18540214-18540228 chr19:18539889-18539903 chr19:18540045-18540056 chr19:18540272-18540286 chr19:18540053-18540064 chr19:18539780-18539794 chr19:18540148-18540162
5	POLR2A	chr19:18538551-18551124	K562	blood:	n/a	n/a
6	POLR2A	chr19:18540605-18540948	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr19:18534926-18553479	K562	blood:	n/a	n/a
8	PML	chr19:18540353-18540834	GM12878	blood:	n/a	n/a
9	RCOR1	chr19:18540614-18540781	GM12878	blood:	n/a	n/a
10	POLR2A	chr19:18539579-18540941	PANC-1	pancreas:	n/a	n/a
11	ZNF143	chr19:18540344-18540978	H1-hESC	embryonic stem cell:	n/a	n/a
12	STAT5A	chr19:18539508-18541125	GM12878	blood:	n/a	chr19:18540393-18540405 chr19:18540676-18540688 chr19:18540276-18540288 chr19:18540471-18540483 chr19:18540966-18540978 chr19:18540020-18540032 chr19:18540053-18540065 chr19:18540277-18540289 chr19:18540618-18540630
13	POLR2A	chr19:18540606-18540829	GM12878	blood:	n/a	n/a
14	CBX3	chr19:18540642-18540981	K562	blood:	n/a	n/a
15	POLR2A	chr19:18540643-18541031	PFSK-1	brain:	n/a	n/a
16	MAX	chr19:18540431-18540680	K562	blood:	n/a	chr19:18540468-18540478
17	NFATC1	chr19:18540174-18540991	GM12878	blood:	n/a	n/a
18	POLR2A	chr19:18539600-18541000	K562	blood:	n/a	n/a
19	POLR2A	chr19:18540510-18540898	GM12891	blood:	n/a	n/a
20	NR2F2	chr19:18540546-18540820	K562	blood:	n/a	n/a
21	MTA3	chr19:18539376-18541026	GM12878	blood:	n/a	n/a
22	ZBTB7A	chr19:18539739-18540950	K562	blood:	n/a	chr19:18540747-18540755
23	POLR2A	chr19:18539447-18540987	GM12892	blood:	n/a	n/a
24	RUNX3	chr19:18540424-18540994	GM12878	blood:	n/a	chr19:18540910-18540925
25	ZBTB7A	chr19:18539659-18540916	K562	blood:	n/a	chr19:18540747-18540755
26	ZBTB7A	chr19:18539829-18540865	ECC-1	luminal epithelium:	n/a	chr19:18540747-18540755
27	POLR2A	chr19:18539622-18542014	K562	blood:	n/a	n/a
28	ZNF263	chr19:18540558-18540882	HEK293-T-REx	kidney:	n/a	chr19:18540669-18540690
29	POLR2A	chr19:18540583-18540872	GM12878	blood:	n/a	n/a
30	ELF1	chr19:18539487-18540848	GM12878	blood:	n/a	chr19:18539538-18539550 chr19:18539896-18539908
31	MAZ	chr19:18538890-18540982	IMR90	lung:	n/a	chr19:18540279-18540289 chr19:18539367-18539376 chr19:18540138-18540147 chr19:18539850-18539859 chr19:18540468-18540478
32	RUNX3	chr19:18540498-18540904	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18495232..18499014-chr19:18539147..18542857,5	K562	blood:
2	chr19:18540459..18542781-chr19:18632920..18634658,2	K562	blood:
3	chr19:18538215..18540689-chr19:18541318..18544057,3	MCF-7	breast:
4	chr19:18527431..18533703-chr19:18536573..18544512,11	MCF-7	breast:
5	chr19:18539549..18542308-chr19:18573841..18576282,3	K562	blood:
6	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
7	chr19:18388633..18392429-chr19:18537213..18541674,5	K562	blood:
8	chr19:18385704..18387487-chr19:18538825..18541635,2	K562	blood:

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000267959	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000130511	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10164323	0.85[JPT][hapmap]
rs10401741	0.82[MEX][hapmap]
rs10402322	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10409346	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10409408	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10410797	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10413922	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10416993	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10418331	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10418554	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10420384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10423802	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10426768	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1045631	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11086110	0.88[CEU][hapmap];0.88[CHB][hapmap];0.82[TSI][hapmap];0.90[EUR][1000 genomes]
rs11668704	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11670392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11672385	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11879757	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12980726	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12982295	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12983263	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13344313	0.83[CHD][hapmap]
rs1469412	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1469413	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1971093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2013069	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2162797	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2303692	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28534973	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2891676	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34213500	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.93[JPT][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35004712	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35742476	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4006662	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4303657	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4580317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4808802	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808803	0.94[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808805	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808806	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808807	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808808	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4808811	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808813	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55715336	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57923655	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6512268	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6512269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6512270	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6512271	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7246788	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7247540	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7249760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7251640	1.00[CHB][hapmap]
rs7252130	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7252185	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7255936	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7256530	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7258891	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7259135	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7507218	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8100343	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8102717	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8104247	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8106068	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8106332	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8111397	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8111582	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8111824	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.93[JPT][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8112372	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8112859	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs888668	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
3	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
7	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
8	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
9	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
11	nsv911278	chr19:18526536-18550276	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
12	nsv911279	chr19:18533642-18550276	Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
13	nsv911280	chr19:18533642-18552139	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs888669	ZNF14	cis	parietal	SCAN
rs888669	ISYNA1	cis	parietal	SCAN
rs888669	SSBP4	cis	multi-tissue	Pritchard
rs888669	ABHD8	cis	parietal	SCAN
rs888669	LOC646044///SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs888669	CHERP	cis	cerebellum	SCAN
rs888669	ZNF93	cis	cerebellum	SCAN
rs888669	SSBP4	cis	lymphoblastoid	seeQTL
rs888669	SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs888669	SSBP4	cis	Lymphoblastoid	GTEx
rs888669	CYP4F11	cis	parietal	SCAN

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18531400-18543000	Enhancers	Fetal Brain Male	brain
2	chr19:18532800-18547600	Weak transcription	HepG2	liver
3	chr19:18533800-18541000	Enhancers	Placenta	Placenta
4	chr19:18536200-18541200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:18536600-18542200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr19:18537400-18541600	Genic enhancers	NHLF	lung
7	chr19:18537400-18543800	Weak transcription	NHEK	skin
8	chr19:18537400-18544000	Weak transcription	HMEC	breast
9	chr19:18538000-18547600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:18538000-18548400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:18539000-18541200	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr19:18539200-18540800	Flanking Active TSS	Fetal Brain Female	brain
13	chr19:18539200-18541000	Enhancers	Fetal Lung	lung
14	chr19:18539200-18541000	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr19:18539200-18541000	Enhancers	NHDF-Ad	bronchial
16	chr19:18539200-18541600	Enhancers	Stomach Mucosa	stomach
17	chr19:18539200-18544000	Enhancers	Fetal Heart	heart
18	chr19:18539400-18541000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:18539600-18540800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr19:18539600-18540800	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr19:18539600-18540800	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr19:18539600-18540800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr19:18539600-18540800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr19:18539600-18540800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr19:18539600-18540800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
26	chr19:18539600-18540800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:18539600-18540800	Flanking Active TSS	Dnd41	blood
28	chr19:18539600-18540800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr19:18539600-18540800	Flanking Active TSS	NH-A	brain
30	chr19:18539600-18541000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr19:18539600-18541000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr19:18539600-18541000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr19:18539600-18541000	Enhancers	Lung	lung
34	chr19:18539600-18541000	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr19:18539600-18541000	Enhancers	HSMMtube	muscle
36	chr19:18539600-18541400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr19:18539800-18540800	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr19:18539800-18540800	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr19:18539800-18541000	Active TSS	H9 Cell Line	embryonic stem cell
40	chr19:18540000-18541000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr19:18540000-18541000	Enhancers	Pancreas	Pancrea
42	chr19:18540000-18541000	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr19:18540000-18541000	Active TSS	Rectal Smooth Muscle	rectum
44	chr19:18540000-18541000	Enhancers	Spleen	Spleen
45	chr19:18540200-18540800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr19:18540200-18540800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
47	chr19:18540200-18540800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr19:18540200-18540800	Enhancers	Adipose Nuclei	Adipose
49	chr19:18540200-18540800	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr19:18540200-18540800	Flanking Active TSS	Brain Germinal Matrix	brain

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