Variant report

Variant	rs10410698
Chromosome Location	chr19:42783355-42783356
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	POLR2A	chr19:42783224-42783509	Hela-S3	cervix:	n/a	n/a
2	ETS1	chr19:42783344-42784802	A549	lung:	n/a	chr19:42784030-42784043 chr19:42784101-42784112
3	POLR2A	chr19:42783290-42786530	K562	blood:	n/a	n/a
4	ATF3	chr19:42783212-42785007	A549	lung:	n/a	chr19:42784295-42784304 chr19:42784977-42784986 chr19:42784547-42784556 chr19:42784588-42784597
5	SIX5	chr19:42782692-42785106	A549	lung:	n/a	n/a
6	RAD21	chr19:42783252-42785037	SK-N-SH	brain:	n/a	chr19:42784058-42784072 chr19:42784086-42784099 chr19:42784087-42784097 chr19:42784555-42784569 chr19:42783408-42783421
7	POLR2A	chr19:42782865-42784912	HepG2	liver:	n/a	n/a
8	CTCF	chr19:42783340-42783490	BJ	skin:	n/a	chr19:42783407-42783420
9	CTCF	chr19:42781622-42785846	A549	lung:	n/a	chr19:42784097-42784110 chr19:42783407-42783420 chr19:42783100-42783113 chr19:42784251-42784264 chr19:42782182-42782200 chr19:42784085-42784103 chr19:42784087-42784100 chr19:42782184-42782205 chr19:42783097-42783115
10	POLR2A	chr19:42783093-42783590	HepG2	liver:	n/a	n/a
11	POLR2A	chr19:42783321-42783673	GM12891	blood:	n/a	n/a
12	POLR2A	chr19:42781501-42785091	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr19:42782012-42786927	U87	brain:	n/a	n/a
14	POLR2A	chr19:42783347-42783566	GM12878	blood:	n/a	n/a
15	POLR2A	chr19:42783313-42786769	K562	blood:	n/a	n/a
16	TCF12	chr19:42783241-42785257	A549	lung:	n/a	chr19:42784112-42784122 chr19:42783464-42783474 chr19:42785031-42785038 chr19:42783818-42783826 chr19:42784035-42784045
17	POLR2A	chr19:42783262-42786908	U87	brain:	n/a	n/a
18	POLR2A	chr19:42781915-42785217	PFSK-1	brain:	n/a	n/a
19	POLR2A	chr19:42781785-42788117	SK-N-MC	brain:	n/a	n/a
20	CTCF	chr19:42783280-42783430	GM12875	blood:	n/a	chr19:42783407-42783420
21	FOSL2	chr19:42783279-42785354	A549	lung:	n/a	chr19:42784334-42784343 chr19:42784633-42784642 chr19:42785178-42785190 chr19:42784663-42784672 chr19:42785180-42785188
22	POLR2A	chr19:42783022-42785209	HepG2	liver:	n/a	n/a
23	POLR2A	chr19:42782913-42785033	GM12878	blood:	n/a	n/a
24	POLR2A	chr19:42782998-42783650	GM12891	blood:	n/a	n/a
25	MXI1	chr19:42783201-42791351	SK-N-SH	brain:	n/a	chr19:42785246-42785261 chr19:42783290-42783299 chr19:42786708-42786717 chr19:42783465-42783474 chr19:42784488-42784503
26	REST	chr19:42783220-42785068	A549	lung:	n/a	chr19:42784059-42784077 chr19:42784035-42784048 chr19:42784965-42784978
27	SMC3	chr19:42783296-42785206	SK-N-SH	brain:	n/a	chr19:42784087-42784101 chr19:42784087-42784097 chr19:42785143-42785151 chr19:42784100-42784110
28	BCL3	chr19:42783261-42788037	A549	lung:	n/a	chr19:42784292-42784305 chr19:42784099-42784112 chr19:42785738-42785746 chr19:42785147-42785160 chr19:42784294-42784303 chr19:42784104-42784113 chr19:42784556-42784569

No.	Distal block	Cell Line	Cell type
1	chr19:42744297..42761073-chr19:42776978..42802286,113	MCF-7	breast:
2	chr19:42750067..42750945-chr19:42783006..42783636,2	K562	blood:
3	chr19:42719792..42722067-chr19:42782556..42784868,3	MCF-7	breast:
4	chr19:42743599..42762610-chr19:42780302..42801550,102	MCF-7	breast:
5	chr19:42783298..42787362-chr19:42802681..42808039,8	MCF-7	breast:
6	chr19:42720002..42723178-chr19:42782377..42785942,3	MCF-7	breast:

Variant related genes	Relation type
CIC	TF binding region
ENSG00000204957	Chromatin interaction
ENSG00000268643	Chromatin interaction
ENSG00000160570	Chromatin interaction
ENSG00000105723	Chromatin interaction
ENSG00000105722	Chromatin interaction
ENSG00000079462	Chromatin interaction
ENSG00000188368	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10410185	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10410198	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10412833	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10426306	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10426310	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11557114	0.91[ASN][1000 genomes]
rs11878620	0.82[CHB][hapmap];0.91[ASN][1000 genomes]
rs11880124	0.82[CHB][hapmap]
rs11882654	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11883412	0.82[CHB][hapmap]
rs1206009	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1206027	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.90[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs1206028	0.85[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.85[TSI][hapmap]
rs1206029	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap]
rs1206031	0.80[EUR][1000 genomes]
rs1206033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.89[MEX][hapmap];0.89[TSI][hapmap]
rs1206035	0.84[EUR][1000 genomes]
rs1206038	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs1206040	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.84[EUR][1000 genomes]
rs1206041	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs1206042	0.84[EUR][1000 genomes]
rs1206044	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs1209280	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1211265	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13346991	0.84[EUR][1000 genomes]
rs1613100	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.94[TSI][hapmap];0.82[EUR][1000 genomes]
rs1654623	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.94[TSI][hapmap];0.82[EUR][1000 genomes]
rs1676211	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs1676213	0.82[EUR][1000 genomes]
rs1676215	0.82[EUR][1000 genomes]
rs1676217	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1676220	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1676221	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.84[EUR][1000 genomes]
rs1676222	1.00[CHB][hapmap]
rs1685565	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs16975684	0.82[CHB][hapmap]
rs2267630	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs2302485	0.82[CHB][hapmap];0.91[ASN][1000 genomes]
rs2303652	0.82[CHB][hapmap]
rs2537697	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2615614	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28537976	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28621009	1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs35493131	0.91[ASN][1000 genomes]
rs35557987	0.80[EUR][1000 genomes]
rs3745231	0.82[CHB][hapmap]
rs3745233	0.82[CHB][hapmap]
rs3810148	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3810151	0.82[CHB][hapmap]
rs4141062	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs57938324	1.00[ASN][1000 genomes]
rs7248379	0.82[CHB][hapmap]
rs7255956	0.84[EUR][1000 genomes]
rs7258727	0.86[YRI][hapmap]
rs7258795	1.00[ASN][1000 genomes]
rs7260287	0.84[EUR][1000 genomes]
rs73552881	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73552895	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs741070	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8182491	0.82[CHB][hapmap]
rs851296	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];0.94[TSI][hapmap];0.83[YRI][hapmap];0.82[EUR][1000 genomes]
rs851612	0.95[ASN][1000 genomes]
rs851615	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs862228	0.84[EUR][1000 genomes]
rs865436	0.84[EUR][1000 genomes]
rs9636121	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats 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
3	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
4	nsv911782	chr19:42514712-42931004	Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	esv1794508	chr19:42580026-42791462	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv1055554	chr19:42619671-42821642	Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
7	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
8	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
9	nsv833834	chr19:42736444-42835027	Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	42 gene(s)	inside rSNPs	diseases
10	nsv911784	chr19:42741124-42787664	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
11	nsv911785	chr19:42741124-42917545	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
12	nsv911786	chr19:42744234-42797959	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
13	esv1802977	chr19:42754437-42789945	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases
14	esv1801251	chr19:42768288-42788467	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
15	esv1803455	chr19:42768288-42788467	Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
16	esv1803706	chr19:42768288-42788467	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
17	esv1801291	chr19:42772432-42788467	Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
18	esv1801294	chr19:42772432-42788467	Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
19	esv1801914	chr19:42772432-42788467	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	21 gene(s)	inside rSNPs	diseases
20	nsv911787	chr19:42773862-42795554	Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42774400-42783600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr19:42775800-42783600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:42778200-42783400	Genic enhancers	Fetal Muscle Trunk	muscle
4	chr19:42778400-42783400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:42778400-42783800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:42779000-42783400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr19:42779200-42783400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr19:42779200-42783400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr19:42779200-42783600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr19:42779400-42783400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr19:42779400-42783400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr19:42779400-42783600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr19:42779400-42783800	Enhancers	Right Atrium	heart
14	chr19:42779600-42783400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr19:42779600-42783400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr19:42779600-42783600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr19:42780000-42783800	Enhancers	Psoas Muscle	Psoas
18	chr19:42780200-42783400	Enhancers	Brain Angular Gyrus	brain
19	chr19:42780400-42783400	Enhancers	NHDF-Ad	bronchial
20	chr19:42780400-42783600	Genic enhancers	Fetal Stomach	stomach
21	chr19:42780600-42783800	Enhancers	Left Ventricle	heart
22	chr19:42780600-42783800	Enhancers	Placenta Amnion	Placenta Amnion
23	chr19:42780800-42783400	Weak transcription	Aorta	Aorta
24	chr19:42780800-42783600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:42780800-42783600	Enhancers	Esophagus	oesophagus
26	chr19:42780800-42783600	Genic enhancers	Fetal Intestine Small	intestine
27	chr19:42780800-42783600	Enhancers	Osteobl	bone
28	chr19:42781000-42783600	Enhancers	NH-A	brain
29	chr19:42781200-42783400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr19:42781200-42783400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr19:42781200-42783400	Enhancers	Brain Substantia Nigra	brain
32	chr19:42781200-42783600	Enhancers	Colonic Mucosa	Colon
33	chr19:42781200-42783600	Enhancers	Fetal Brain Male	brain
34	chr19:42781200-42783600	Enhancers	Gastric	stomach
35	chr19:42781200-42783600	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr19:42781200-42783800	Enhancers	Liver	Liver
37	chr19:42781200-42783800	Enhancers	Stomach Mucosa	stomach
38	chr19:42781600-42783400	Enhancers	Brain Cingulate Gyrus	brain
39	chr19:42781600-42783400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr19:42781600-42783400	Enhancers	HepG2	liver
41	chr19:42781600-42783600	Enhancers	Primary hematopoietic stem cells	blood
42	chr19:42781800-42783400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:42781800-42783400	Flanking Active TSS	HSMM	muscle
44	chr19:42781800-42783600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr19:42781800-42783600	Enhancers	Fetal Lung	lung
46	chr19:42781800-42783600	Genic enhancers	NHLF	lung
47	chr19:42781800-42783800	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr19:42781800-42783800	Transcr. at gene 5' and 3'	NHEK	skin
49	chr19:42781800-42784000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr19:42781800-42784000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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