Variant report

Variant	rs7741
Chromosome Location	chr10:5138607-5138608
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	HEY1	chr10:5138348-5138950	HepG2	liver:	n/a	n/a
2	SP1	chr10:5136292-5138992	A549	lung:	n/a	chr10:5136552-5136562 chr10:5136548-5136562 chr10:5136551-5136563 chr10:5136551-5136563 chr10:5136552-5136561 chr10:5136507-5136528
3	POLR2A	chr10:5138306-5138640	A549	lung:	n/a	n/a
4	POLR2A	chr10:5138324-5138880	A549	lung:	n/a	n/a
5	POLR2A	chr10:5138399-5138871	A549	lung:	n/a	n/a
6	SP1	chr10:5137770-5139058	A549	lung:	n/a	n/a
7	REST	chr10:5135146-5139228	A549	lung:	n/a	n/a
8	POLR2A	chr10:5138034-5138918	A549	lung:	n/a	n/a
9	HEY1	chr10:5138310-5138830	HepG2	liver:	n/a	n/a
10	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
11	POLR2A	chr10:5138328-5138856	A549	lung:	n/a	n/a
12	FOSL2	chr10:5135165-5139175	A549	lung:	n/a	chr10:5136821-5136831 chr10:5136823-5136834 chr10:5136821-5136830 chr10:5136821-5136831 chr10:5138903-5138915 chr10:5136822-5136831 chr10:5136820-5136832 chr10:5136822-5136829
13	JUND	chr10:5138319-5139045	A549	lung:	n/a	chr10:5138903-5138915
14	TAF1	chr10:5137827-5139035	A549	lung:	n/a	n/a
15	SIN3AK20	chr10:5137967-5138978	A549	lung:	n/a	n/a
16	TCF12	chr10:5134878-5139332	A549	lung:	n/a	n/a
17	SIX5	chr10:5136756-5139393	A549	lung:	n/a	n/a
18	CTCF	chr10:5136062-5138926	A549	lung:	n/a	chr10:5137004-5137025 chr10:5137015-5137024 chr10:5137009-5137027

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:

Variant related genes	Relation type
ENSG00000239142	TF binding region
ENSG00000196139	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10508294	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10904415	0.82[ASW][hapmap];1.00[CEU][hapmap];0.82[MEX][hapmap];0.97[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10904416	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10904436	0.80[EUR][1000 genomes]
rs10904439	0.81[EUR][1000 genomes]
rs11252928	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11252931	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11252934	1.00[ASW][hapmap];1.00[CEU][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11252935	1.00[CEU][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11252936	1.00[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11252937	1.00[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11252941	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11252955	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11252968	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11252972	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11252978	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11252992	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11253010	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11253012	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11253013	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11253015	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11253016	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11253018	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11253019	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11253020	0.96[CEU][hapmap];0.90[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11253021	0.96[CEU][hapmap];0.90[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11253022	0.96[CEU][hapmap];0.90[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11253036	0.80[EUR][1000 genomes]
rs11253039	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11492955	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11517338	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11517343	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11517344	0.83[AMR][1000 genomes]
rs12354416	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12354530	1.00[CEU][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12357445	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12357449	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12359896	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12360480	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12769156	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1334466	0.86[AMR][1000 genomes]
rs1334467	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1334471	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1334738	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1334739	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17134288	0.96[CEU][hapmap];0.80[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17305952	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1889458	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1937843	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1937909	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2020172	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2210679	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2895061	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2895064	0.85[CEU][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35219485	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3763676	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4448597	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4880711	0.92[CEU][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs4880714	0.82[EUR][1000 genomes]
rs4880715	0.82[EUR][1000 genomes]
rs4881406	0.96[CEU][hapmap];0.80[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4881407	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6601901	0.85[EUR][1000 genomes]
rs6601907	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6601918	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7069331	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7090349	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7090531	0.96[CEU][hapmap];0.80[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7097295	0.96[CEU][hapmap];0.80[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7097646	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7477623	1.00[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7478099	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7920141	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7920454	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9730736	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9794203	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894792	chr10:4832920-5498724	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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	47 gene(s)	inside rSNPs	diseases
2	nsv948794	chr10:4863093-5227382	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1045155	chr10:4872239-5211318	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1040343	chr10:4872814-5196815	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv540462	chr10:4872814-5196815	Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv869470	chr10:4878904-5203685	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv466713	chr10:4901798-5319679	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv549881	chr10:4901798-5319679	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats 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	68 gene(s)	inside rSNPs	diseases
10	nsv1050246	chr10:4927428-5211318	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv549882	chr10:4943518-5203864	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	esv2763913	chr10:4961021-5321407	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv1039386	chr10:5008383-5348491	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv1036566	chr10:5037926-5261426	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv549883	chr10:5037926-5275762	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv1047484	chr10:5076258-5261482	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
17	nsv1036291	chr10:5076258-5456234	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
18	nsv1042487	chr10:5090313-5196900	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv540463	chr10:5090313-5196900	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	nsv540464	chr10:5108345-5196815	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	nsv540465	chr10:5108345-5261482	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
22	nsv540466	chr10:5114577-5196815	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
23	nsv540467	chr10:5114577-5225365	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv540468	chr10:5114577-5261482	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv540469	chr10:5120774-5225365	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv540470	chr10:5120774-5261482	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv540471	chr10:5133561-5261482	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
28	nsv540472	chr10:5133561-5284334	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv947728	chr10:5138057-5138813	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7741	AKR1C3	cis	cerebellum	SCAN
rs7741	AKR1C3	cis	parietal	SCAN

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5136000-5139400	Active TSS	Duodenum Mucosa	Duodenum
2	chr10:5136200-5138800	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr10:5136400-5138800	Active TSS	Brain Anterior Caudate	brain
4	chr10:5136400-5139000	Active TSS	Duodenum Smooth Muscle	Duodenum
5	chr10:5136400-5139000	Active TSS	Rectal Mucosa Donor 31	rectum
6	chr10:5136400-5140000	Active TSS	Right Atrium	heart
7	chr10:5136600-5138800	Active TSS	Stomach Mucosa	stomach
8	chr10:5136600-5147400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr10:5137000-5138800	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr10:5137000-5141200	Weak transcription	Lung	lung
11	chr10:5137200-5145200	Weak transcription	Esophagus	oesophagus
12	chr10:5137200-5145800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr10:5137200-5149800	Weak transcription	Small Intestine	intestine
14	chr10:5137400-5149400	Weak transcription	HSMM	muscle
15	chr10:5137400-5149600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr10:5137400-5149600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr10:5137400-5149800	Weak transcription	Pancreas	Pancrea
18	chr10:5137400-5151600	Weak transcription	Brain Angular Gyrus	brain
19	chr10:5137400-5151800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr10:5137400-5152000	Weak transcription	Right Ventricle	heart
21	chr10:5137600-5141600	Weak transcription	Brain Substantia Nigra	brain
22	chr10:5137600-5147800	Weak transcription	HMEC	breast
23	chr10:5137800-5141800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr10:5137800-5150800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:5138000-5139000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr10:5138000-5147200	Transcr. at gene 5' and 3'	A549	lung
27	chr10:5138200-5138800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr10:5138200-5138800	Enhancers	Thymus	Thymus
29	chr10:5138200-5146800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr10:5138200-5148400	Weak transcription	Brain Cingulate Gyrus	brain
31	chr10:5138200-5151000	Weak transcription	Osteobl	bone
32	chr10:5138200-5151800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr10:5138400-5138800	Active TSS	Colonic Mucosa	Colon
34	chr10:5138400-5138800	Flanking Active TSS	NHDF-Ad	bronchial
35	chr10:5138400-5139000	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr10:5138400-5139000	Flanking Active TSS	Hela-S3	cervix
37	chr10:5138400-5139600	Weak transcription	Primary hematopoietic stem cells	blood
38	chr10:5138400-5139600	Transcr. at gene 5' and 3'	HepG2	liver
39	chr10:5138400-5140200	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:5138400-5141200	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:5138600-5138800	Enhancers	Aorta	Aorta
42	chr10:5138600-5138800	Active TSS	Liver	Liver
43	chr10:5138600-5138800	Enhancers	Colon Smooth Muscle	Colon
44	chr10:5138600-5138800	Enhancers	Psoas Muscle	Psoas
45	chr10:5138600-5138800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr10:5138600-5139000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr10:5138600-5139600	Weak transcription	Left Ventricle	heart
48	chr10:5138600-5139600	Weak transcription	HSMMtube	muscle
49	chr10:5138600-5140800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:5138600-5140800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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