Variant report

Variant	rs198826
Chromosome Location	chr6:26121153-26121154
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	FOXA1	chr6:26121101-26121901	HepG2	liver:	n/a	chr6:26121444-26121456 chr6:26121575-26121587
2	MYBL2	chr6:26121136-26122231	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:26121111-26122077	HepG2	liver:	n/a	n/a
4	FOXA2	chr6:26120969-26122126	HepG2	liver:	n/a	chr6:26121444-26121456 chr6:26121575-26121587
5	TCF12	chr6:26121043-26121950	A549	lung:	n/a	n/a
6	MBD4	chr6:26120830-26122002	HepG2	liver:	n/a	n/a
7	IRF3	chr6:26121071-26121275	GM12878	blood:	n/a	chr6:26121145-26121162 chr6:26121148-26121162
8	POLR2A	chr6:26112014-26135800	K562	blood:	n/a	n/a
9	FOSL2	chr6:26121104-26122067	A549	lung:	n/a	chr6:26121702-26121709 chr6:26121761-26121770 chr6:26121360-26121372 chr6:26121545-26121554 chr6:26121162-26121171 chr6:26121702-26121711
10	MYBL2	chr6:26120835-26125191	HepG2	liver:	n/a	n/a
11	HEY1	chr6:26121044-26122151	HepG2	liver:	n/a	n/a
12	TEAD4	chr6:26120905-26127941	K562	blood:	n/a	n/a
13	POLR2A	chr6:26121097-26122088	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:26120221-26136970	K562	blood:	n/a	n/a
15	POLR2A	chr6:26121111-26122105	HepG2	liver:	n/a	n/a
16	NFIC	chr6:26120879-26124973	HepG2	liver:	n/a	n/a
17	CUX1	chr6:26121094-26121916	K562	blood:	n/a	n/a
18	YY1	chr6:26121087-26121419	HepG2	liver:	n/a	chr6:26121223-26121233
19	FOXA1	chr6:26121119-26121959	HepG2	liver:	n/a	chr6:26121444-26121456 chr6:26121575-26121587
20	POLR2A	chr6:26121000-26129264	H1-hESC	embryonic stem cell:	n/a	n/a
21	SP1	chr6:26121069-26122086	A549	lung:	n/a	chr6:26121855-26121869
22	BCLAF1	chr6:26120463-26129092	K562	blood:	n/a	chr6:26126779-26126788 chr6:26122722-26122731 chr6:26125896-26125905
23	HEY1	chr6:26121111-26129034	K562	blood:	n/a	n/a
24	EP300	chr6:26121140-26121876	A549	lung:	n/a	chr6:26121574-26121584 chr6:26121702-26121711 chr6:26121164-26121173
25	EP300	chr6:26121080-26121945	HepG2	liver:	n/a	chr6:26121574-26121584 chr6:26121702-26121711 chr6:26121164-26121173

No.	Distal block	Cell Line	Cell type
1	chr6:26120892..26123580-chr6:27107524..27109236,2	K562	blood:
2	chr6:26120836..26126141-chr6:27110374..27116911,13	K562	blood:
3	chr6:26119733..26121596-chr6:27838057..27840229,2	MCF-7	breast:
4	chr6:24763238..24766059-chr6:26119737..26122473,2	K562	blood:
5	chr6:26119257..26128074-chr6:27097161..27104707,27	K562	blood:
6	chr3:72142216..72143736-chr6:26119290..26121939,2	MCF-7	breast:
7	chr6:26119863..26128842-chr6:27096583..27102911,26	K562	blood:
8	chr6:26017750..26036418-chr6:26116875..26130553,65	MCF-7	breast:
9	chr6:26053512..26063692-chr6:26116837..26127451,29	MCF-7	breast:
10	chr17:56707835..56709463-chr6:26118684..26121673,2	MCF-7	breast:

Variant related genes	Relation type
HIST1H2AC	TF binding region
ENSG00000124635	Chromatin interaction
ENSG00000182572	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000124610	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000184825	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1056314	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13161	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1572982	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs198800	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs198803	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198807	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198809	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.97[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198813	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198814	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198816	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198817	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198819	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap]
rs198821	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198822	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198823	0.83[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap]
rs198824	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198825	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198828	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.95[LWK][hapmap];0.96[MEX][hapmap];0.98[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198829	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198830	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198831	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs198835	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs198836	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs198837	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs198838	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs198840	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs198841	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs198842	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs198843	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs198844	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs198854	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs198856	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs198857	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs198858	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2071303	0.83[CHD][hapmap]
rs6918586	0.94[ASW][hapmap];0.87[MKK][hapmap];0.89[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
8	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
9	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
10	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
11	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
12	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
13	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
14	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
15	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
16	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
17	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
18	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs198826	ZNF165	cis	parietal	SCAN
rs198826	HIST1H2BM	cis	cerebellum	SCAN
rs198826	HIST1H2AJ	cis	parietal	SCAN
rs198826	HIST1H1T	cis	multi-tissue	Pritchard

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26104800-26122600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:26105000-26122600	Weak transcription	Right Atrium	heart
3	chr6:26107600-26122800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:26108400-26121200	Weak transcription	Fetal Intestine Small	intestine
5	chr6:26110400-26122600	Weak transcription	Primary B cells from cord blood	blood
6	chr6:26114200-26121800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:26115800-26122400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:26115800-26122400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:26115800-26122600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:26116000-26121200	Weak transcription	Stomach Mucosa	stomach
11	chr6:26116200-26121600	Weak transcription	Primary T cells from cord blood	blood
12	chr6:26116800-26121400	Weak transcription	Thymus	Thymus
13	chr6:26119400-26122400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:26119400-26122600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:26119400-26122600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:26119600-26121200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:26119600-26121200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:26119600-26121200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:26119600-26121200	Active TSS	K562	blood
20	chr6:26119600-26121200	Weak transcription	NH-A	brain
21	chr6:26119600-26121400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:26119600-26122400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr6:26119600-26122400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr6:26119600-26122400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:26119600-26122400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:26119600-26122600	Weak transcription	Brain Anterior Caudate	brain
27	chr6:26119600-26122600	Weak transcription	Brain Hippocampus Middle	brain
28	chr6:26119600-26123400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:26119800-26121200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:26119800-26121400	Weak transcription	HMEC	breast
31	chr6:26119800-26122600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr6:26119800-26122600	Weak transcription	Brain Substantia Nigra	brain
33	chr6:26120200-26122400	Enhancers	Fetal Thymus	thymus
34	chr6:26120400-26121800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:26120600-26122000	Enhancers	Small Intestine	intestine
36	chr6:26120600-26122400	Enhancers	Dnd41	blood
37	chr6:26120800-26121400	Flanking Active TSS	Liver	Liver
38	chr6:26120800-26121400	Enhancers	Fetal Kidney	kidney
39	chr6:26120800-26121600	Enhancers	Brain Cingulate Gyrus	brain
40	chr6:26120800-26122400	Active TSS	A549	lung
41	chr6:26120800-26122800	Flanking Active TSS	HepG2	liver
42	chr6:26121000-26121200	Enhancers	Duodenum Mucosa	Duodenum
43	chr6:26121000-26122000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr6:26121000-26122000	Flanking Active TSS	GM12878-XiMat	blood
45	chr6:26121000-26122400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:26121000-26122600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:26121000-26122600	Enhancers	Fetal Intestine Large	intestine

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