Variant report

Variant	rs3740324
Chromosome Location	chr10:43047310-43047311
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr10:43046914-43048474	HEK293-T-REx	kidney:	n/a	n/a
2	MAX	chr10:43047005-43048774	K562	blood:	n/a	n/a
3	KAP1	chr10:43047250-43048854	HEK293	kidney:	n/a	n/a
4	E2F6	chr10:43047067-43047999	K562	blood:	n/a	chr10:43047814-43047825
5	MXI1	chr10:43047264-43048754	HepG2	liver:	n/a	n/a
6	E2F6	chr10:43047097-43048440	K562	blood:	n/a	chr10:43047814-43047825
7	MAX	chr10:43047225-43048899	HepG2	liver:	n/a	n/a
8	POLR2A	chr10:43047167-43048799	K562	blood:	n/a	n/a
9	ELF1	chr10:43047303-43048874	GM12878	blood:	n/a	chr10:43048602-43048613
10	MAX	chr10:43047206-43049183	HepG2	liver:	n/a	n/a
11	E2F6	chr10:43047265-43048191	A549	lung:	n/a	chr10:43047814-43047825
12	MAX	chr10:43047234-43048898	A549	lung:	n/a	n/a
13	MAX	chr10:43047307-43048863	MCF-7	breast:	n/a	n/a
14	POLR2A	chr10:43047044-43047359	HepG2	liver:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43046301..43049301-chr10:43278095..43279962,3	K562	blood:
2	chr10:43043951..43049889-chr10:43132519..43135803,5	K562	blood:
3	chr10:43046145..43048386-chr10:43132522..43135382,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-4	chr10:43047025-43048044	NONHSAT012891
2	lnc-ZNF33B-4	chr10:43047025-43047739	NONHSAT012893
3	lnc-ZNF33B-4	chr10:43047025-43048236	NONHSAT012894
4	lnc-ZNF33B-4	chr10:43047021-43048044	NONHSAT012901

No data

Variant related genes	Relation type
FXYD6P1	TF binding region
ENSG00000165733	Chromatin interaction
ENSG00000196693	Chromatin interaction
ENSG00000272373	Chromatin interaction

Extended variants
information (count: 160 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:140)

rs_ID	r²[population]
rs10128322	0.87[CEU][hapmap]
rs10900240	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10900251	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10900253	1.00[CEU][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs11239619	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11239621	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11239622	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11239639	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11239642	0.82[EUR][1000 genomes]
rs11239643	0.82[EUR][1000 genomes]
rs11239644	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11239651	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11239653	0.82[EUR][1000 genomes]
rs11239661	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11239662	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11239663	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11239668	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239669	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239670	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239671	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239672	0.87[EUR][1000 genomes]
rs11239675	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11239682	0.86[EUR][1000 genomes]
rs11239707	0.87[EUR][1000 genomes]
rs11239708	0.85[EUR][1000 genomes]
rs11239709	0.87[EUR][1000 genomes]
rs1136118	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11528472	0.83[EUR][1000 genomes]
rs11528550	0.80[EUR][1000 genomes]
rs11528552	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12217930	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12218051	0.86[EUR][1000 genomes]
rs12218419	0.82[EUR][1000 genomes]
rs12219232	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12221072	0.82[EUR][1000 genomes]
rs12221408	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12240565	1.00[CEU][hapmap]
rs12242735	0.87[EUR][1000 genomes]
rs12245618	0.81[EUR][1000 genomes]
rs12256867	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12257762	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12257897	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12259767	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12261023	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12261168	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12262549	0.90[EUR][1000 genomes]
rs12263651	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12266387	0.87[EUR][1000 genomes]
rs12268359	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12771775	0.86[EUR][1000 genomes]
rs1413393	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs158369	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs158379	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs158386	0.92[EUR][1000 genomes]
rs1591248	1.00[CEU][hapmap]
rs17157474	0.86[EUR][1000 genomes]
rs17343205	0.88[CEU][hapmap]
rs17427443	0.85[CEU][hapmap]
rs17428442	0.87[CEU][hapmap]
rs1830491	0.81[EUR][1000 genomes]
rs1831910	0.87[EUR][1000 genomes]
rs1831916	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1855448	0.86[EUR][1000 genomes]
rs1855449	0.86[EUR][1000 genomes]
rs2005977	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2005978	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2016696	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs209378	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs209379	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs209393	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs210219	0.82[CHB][hapmap]
rs210238	0.80[ASN][1000 genomes]
rs210255	0.83[ASN][1000 genomes]
rs2297693	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2419368	1.00[CEU][hapmap];0.93[YRI][hapmap];0.93[EUR][1000 genomes]
rs2505883	0.82[YRI][hapmap]
rs28404481	0.87[EUR][1000 genomes]
rs3740325	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3740327	0.82[EUR][1000 genomes]
rs3740328	0.86[EUR][1000 genomes]
rs3758512	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs3758513	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55904273	0.82[EUR][1000 genomes]
rs55914715	0.87[EUR][1000 genomes]
rs58635980	0.87[EUR][1000 genomes]
rs58877883	0.87[EUR][1000 genomes]
rs60433789	0.87[EUR][1000 genomes]
rs6593371	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6593413	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs66635049	0.86[EUR][1000 genomes]
rs672073	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs672077	0.88[EUR][1000 genomes]
rs7068874	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7069467	0.85[EUR][1000 genomes]
rs7069663	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7071990	0.87[EUR][1000 genomes]
rs7074806	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7075245	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7076534	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7078390	0.87[EUR][1000 genomes]
rs7079577	0.86[EUR][1000 genomes]
rs7079581	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7082367	0.87[EUR][1000 genomes]
rs7082480	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7083254	0.86[EUR][1000 genomes]
rs7085956	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7097766	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7098574	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7100293	0.84[EUR][1000 genomes]
rs7100856	0.85[EUR][1000 genomes]
rs73260601	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73262610	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73262631	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73266634	0.93[EUR][1000 genomes]
rs74137908	0.87[EUR][1000 genomes]
rs74137911	0.87[EUR][1000 genomes]
rs74137912	0.87[EUR][1000 genomes]
rs74137913	0.87[EUR][1000 genomes]
rs74137929	0.81[EUR][1000 genomes]
rs7476285	0.85[EUR][1000 genomes]
rs7899665	0.86[EUR][1000 genomes]
rs7900972	0.92[EUR][1000 genomes]
rs7903632	0.87[EUR][1000 genomes]
rs7904627	0.93[EUR][1000 genomes]
rs7905834	0.88[CEU][hapmap]
rs7906532	0.81[EUR][1000 genomes]
rs7910969	0.93[EUR][1000 genomes]
rs7911986	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7912057	0.86[EUR][1000 genomes]
rs7914365	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7914372	0.80[EUR][1000 genomes]
rs7916307	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7917276	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7918447	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7919880	0.93[EUR][1000 genomes]
rs7920292	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7920620	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7921571	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7921658	0.86[EUR][1000 genomes]
rs9730806	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817455	chr10:42607635-43151812	Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv550670	chr10:42725663-43089965	Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv550672	chr10:42753190-43441729	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS 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	40 gene(s)	inside rSNPs	diseases
4	nsv895054	chr10:42761931-43068841	ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv895064	chr10:42783481-43243325	Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv466877	chr10:42794125-43066414	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv550683	chr10:42794125-43066414	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv533331	chr10:42830221-43356410	ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1042764	chr10:42846383-43511712	Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv895071	chr10:42864138-43066414	ZNF genes & repeats Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv895073	chr10:42884169-43066505	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv1050394	chr10:42890663-43604956	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
13	nsv540573	chr10:42890663-43604956	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
14	nsv534548	chr10:42890664-43729688	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active 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	56 gene(s)	inside rSNPs	diseases
15	nsv469725	chr10:42965130-43178323	Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
16	nsv482513	chr10:42965130-43178323	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
17	esv2758216	chr10:42965131-43510191	Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
18	esv2759746	chr10:42965131-43510191	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
19	nsv948326	chr10:43045385-43047970	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv8625	chr10:43046814-43052296	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS 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

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43035000-43047400	Weak transcription	Stomach Mucosa	stomach
2	chr10:43043200-43047400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr10:43044800-43047400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr10:43046200-43048000	Flanking Active TSS	Dnd41	blood
5	chr10:43046600-43047800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
6	chr10:43046600-43047800	Flanking Active TSS	Fetal Brain Female	brain
7	chr10:43046800-43047400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr10:43046800-43047400	Enhancers	Primary hematopoietic stem cells	blood
9	chr10:43046800-43047400	Enhancers	Small Intestine	intestine
10	chr10:43046800-43047400	Enhancers	Spleen	Spleen
11	chr10:43046800-43047600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:43046800-43047600	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr10:43046800-43047600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr10:43046800-43047600	Flanking Active TSS	HepG2	liver
15	chr10:43046800-43047800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr10:43046800-43047800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr10:43046800-43047800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr10:43046800-43047800	Flanking Active TSS	Brain Angular Gyrus	brain
19	chr10:43046800-43047800	Flanking Active TSS	Brain Cingulate Gyrus	brain
20	chr10:43046800-43047800	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr10:43046800-43047800	Flanking Active TSS	GM12878-XiMat	blood
22	chr10:43046800-43047800	Flanking Active TSS	Hela-S3	cervix
23	chr10:43046800-43048000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr10:43046800-43048000	Flanking Active TSS	K562	blood
25	chr10:43047000-43047400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:43047000-43047400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:43047000-43047400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr10:43047000-43047400	Enhancers	Fetal Intestine Large	intestine
29	chr10:43047000-43047400	Enhancers	Right Atrium	heart
30	chr10:43047000-43047600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr10:43047000-43047600	Flanking Active TSS	Primary T cells from cord blood	blood
32	chr10:43047000-43047600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr10:43047000-43047600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr10:43047000-43047600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:43047000-43047600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr10:43047000-43047600	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr10:43047000-43047600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:43047000-43047600	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr10:43047000-43047600	Flanking Active TSS	Gastric	stomach
40	chr10:43047000-43047600	Flanking Active TSS	Ovary	ovary
41	chr10:43047000-43047600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
42	chr10:43047000-43047600	Flanking Active TSS	NHDF-Ad	bronchial
43	chr10:43047000-43047600	Flanking Active TSS	NHEK	skin
44	chr10:43047000-43047800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr10:43047000-43047800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr10:43047000-43047800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr10:43047000-43047800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr10:43047000-43047800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr10:43047000-43047800	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr10:43047000-43047800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links