Variant report

Variant	rs2993579
Chromosome Location	chr13:95954698-95954699
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	NR2F2	chr13:95954292-95954896	K562	blood:	n/a	n/a
2	MYC	chr13:95952515-95954753	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
3	MYC	chr13:95952780-95954797	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
4	E2F6	chr13:95952942-95954739	H1-hESC	embryonic stem cell:	n/a	chr13:95953182-95953191 chr13:95954182-95954189 chr13:95953447-95953457 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
5	JUN	chr13:95952928-95954771	K562	blood:	n/a	chr13:95953347-95953361 chr13:95953183-95953192
6	MAX	chr13:95953643-95954706	K562	blood:	n/a	chr13:95953997-95954007 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
7	NFATC1	chr13:95954354-95954764	GM12878	blood:	n/a	n/a
8	GATA1	chr13:95952723-95954796	PBDE	blood:	n/a	chr13:95954516-95954525 chr13:95953003-95953015
9	RELA	chr13:95951446-95954754	GM12891	blood:	n/a	chr13:95952082-95952091 chr13:95952082-95952091
10	MXI1	chr13:95952280-95955341	IMR90	lung:	n/a	chr13:95954536-95954545
11	IRF1	chr13:95953702-95954728	K562	blood:	n/a	chr13:95954467-95954481 chr13:95954018-95954025 chr13:95953741-95953755
12	POLR2A	chr13:95951417-95955074	PBDE	blood:	n/a	n/a
13	MAX	chr13:95952944-95954779	H1-hESC	embryonic stem cell:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
14	MAX	chr13:95952929-95954740	SK-N-SH	brain:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
15	MYC	chr13:95952653-95954934	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
16	MAX	chr13:95952612-95954731	A549	lung:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
17	TEAD4	chr13:95954002-95954720	K562	blood:	n/a	n/a
18	E2F6	chr13:95952942-95954719	H1-hESC	embryonic stem cell:	n/a	chr13:95953182-95953191 chr13:95954182-95954189 chr13:95953447-95953457 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
19	MXI1	chr13:95952426-95955290	SK-N-SH	brain:	n/a	chr13:95954536-95954545
20	MAX	chr13:95952775-95954761	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
21	MAX	chr13:95952864-95954734	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
22	RCOR1	chr13:95952757-95954764	K562	blood:	n/a	n/a
23	CHD1	chr13:95952300-95954946	IMR90	lung:	n/a	chr13:95954182-95954189 chr13:95953205-95953215 chr13:95953384-95953394
24	MAX	chr13:95953048-95954762	H1-hESC	embryonic stem cell:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
25	MYC	chr13:95952904-95954709	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
26	E2F6	chr13:95952808-95954774	K562	blood:	n/a	chr13:95953182-95953191 chr13:95954182-95954189 chr13:95953447-95953457 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
27	E2F6	chr13:95953569-95954728	A549	lung:	n/a	chr13:95954182-95954189 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
28	NRF1	chr13:95952890-95954834	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:

Variant related genes	Relation type
ABCC4	TF binding region

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11843664	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12560549	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1764417	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1764419	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2992902	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2992903	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2992905	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2992907	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2992908	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2992909	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2992910	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2993581	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2993582	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2993583	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2993584	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2993585	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61974974	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6650325	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8001444	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs869951	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs871052	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9302056	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9302058	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9524895	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9524896	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533659	chr13:95757713-96042149	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1043019	chr13:95924585-96152616	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv900926	chr13:95927386-95972496	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv900927	chr13:95927386-95975185	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv456078	chr13:95929888-95972496	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv562770	chr13:95929888-95972496	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv900929	chr13:95930072-95972496	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv900930	chr13:95930072-95975185	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1037673	chr13:95930191-96146554	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv541882	chr13:95930191-96146554	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv900931	chr13:95930685-95972496	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1039391	chr13:95931369-96038728	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv471169	chr13:95931992-95972496	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv517610	chr13:95931992-96035883	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription 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	6 gene(s)	inside rSNPs	diseases
15	nsv1047208	chr13:95935757-96036053	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv1044162	chr13:95936858-96032829	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv1044131	chr13:95939874-96016445	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
18	nsv1040348	chr13:95939874-96032829	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv1042622	chr13:95939874-96038728	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	esv2829991	chr13:95942492-95981856	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	esv3693403	chr13:95942492-95981856	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv456079	chr13:95942492-96027507	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
23	nsv562771	chr13:95942492-96027507	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
24	nsv1049988	chr13:95942492-96038728	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
25	nsv1036031	chr13:95943731-96030662	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv1053262	chr13:95943731-96032829	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
27	nsv456080	chr13:95943885-96015129	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
28	nsv562772	chr13:95943885-96015129	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
29	nsv456081	chr13:95943885-96027507	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
30	nsv562773	chr13:95943885-96027507	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
31	nsv1047902	chr13:95945118-96032829	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
32	nsv562774	chr13:95951593-96027507	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95952400-95954800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:95952400-95954800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr13:95952800-95954800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr13:95953800-95954800	Flanking Active TSS	Stomach Smooth Muscle	stomach
5	chr13:95953800-95955400	Flanking Active TSS	K562	blood
6	chr13:95954000-95954800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr13:95954000-95954800	Flanking Active TSS	GM12878-XiMat	blood
8	chr13:95954000-95954800	Flanking Active TSS	Hela-S3	cervix
9	chr13:95954000-95955400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr13:95954200-95954800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:95954200-95954800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
12	chr13:95954200-95954800	Enhancers	Lung	lung
13	chr13:95954400-95954800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr13:95954400-95954800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr13:95954400-95954800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr13:95954400-95954800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr13:95954400-95954800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr13:95954400-95954800	Bivalent Enhancer	Fetal Brain Male	brain
19	chr13:95954400-95955200	Bivalent Enhancer	Brain Germinal Matrix	brain
20	chr13:95954400-95955400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:95954400-95956600	Weak transcription	Right Atrium	heart
22	chr13:95954600-95954800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
23	chr13:95954600-95954800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
24	chr13:95954600-95954800	Active TSS	Primary T cells from cord blood	blood
25	chr13:95954600-95954800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr13:95954600-95954800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr13:95954600-95954800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr13:95954600-95954800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr13:95954600-95954800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr13:95954600-95954800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
31	chr13:95954600-95954800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr13:95954600-95954800	Enhancers	Fetal Intestine Large	intestine
33	chr13:95954600-95954800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr13:95954600-95954800	Transcr. at gene 5' and 3'	A549	lung
35	chr13:95954600-95954800	Enhancers	HMEC	breast
36	chr13:95954600-95954800	Enhancers	HUVEC	blood vessel
37	chr13:95954600-95955200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr13:95954600-95955200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr13:95954600-95955200	Enhancers	Brain Substantia Nigra	brain
40	chr13:95954600-95955600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr13:95954600-95956000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:95954600-95957800	Enhancers	Fetal Intestine Small	intestine
43	chr13:95954600-95958200	Weak transcription	NHLF	lung

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