Variant report

Variant	rs10410606
Chromosome Location	chr19:41108975-41108976
allele	A/C
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	FOSL2	chr19:41107922-41112397	A549	lung:	n/a	chr19:41110415-41110427
2	CTCF	chr19:41107334-41112542	A549	lung:	n/a	chr19:41110180-41110196 chr19:41108676-41108684 chr19:41108186-41108199 chr19:41108187-41108196 chr19:41110184-41110194 chr19:41108671-41108689 chr19:41108181-41108199 chr19:41108183-41108196 chr19:41108666-41108687 chr19:41108184-41108194
3	CTCF	chr19:41106613-41109003	SK-N-SH	brain:	n/a	chr19:41108676-41108684 chr19:41108186-41108199 chr19:41108187-41108196 chr19:41108671-41108689 chr19:41108181-41108199 chr19:41108183-41108196 chr19:41108666-41108687 chr19:41108184-41108194
4	TCF12	chr19:41107775-41112752	A549	lung:	n/a	chr19:41110897-41110905 chr19:41109793-41109800 chr19:41111228-41111238 chr19:41109824-41109831
5	POLR2A	chr19:41107670-41109032	Hela-S3	cervix:	n/a	n/a
6	EP300	chr19:41108903-41109097	K562	blood:	n/a	n/a
7	CTCF	chr19:41108880-41109030	AG10803	skin:	n/a	n/a
8	POLR2A	chr19:41108261-41109307	HUVEC	blood vessel:	n/a	n/a
9	REST	chr19:41107638-41112355	A549	lung:	n/a	chr19:41109783-41109796 chr19:41110030-41110043 chr19:41111216-41111224 chr19:41108709-41108719 chr19:41112104-41112117 chr19:41112227-41112240 chr19:41108218-41108231
10	SIN3AK20	chr19:41108846-41112253	A549	lung:	n/a	n/a
11	CBX3	chr19:41108972-41110071	K562	blood:	n/a	n/a
12	SP1	chr19:41107843-41112596	A549	lung:	n/a	chr19:41110032-41110044 chr19:41111573-41111585 chr19:41110084-41110096 chr19:41112229-41112241 chr19:41112248-41112260 chr19:41110813-41110823 chr19:41108191-41108203 chr19:41110370-41110382 chr19:41112112-41112123 chr19:41110372-41110381 chr19:41110184-41110198 chr19:41110813-41110822 chr19:41111839-41111849 chr19:41109836-41109845 chr19:41108095-41108104 chr19:41110808-41110821 chr19:41110033-41110043 chr19:41111573-41111585 chr19:41109835-41109844 chr19:41110032-41110044 chr19:41108094-41108106 chr19:41110370-41110382 chr19:41110084-41110096 chr19:41109257-41109266 chr19:41108188-41108202 chr19:41108330-41108344 chr19:41112461-41112473 chr19:41108192-41108201 chr19:41112229-41112241 chr19:41110372-41110381 chr19:41110187-41110199 chr19:41110814-41110823 chr19:41109905-41109917 chr19:41110188-41110197 chr19:41110085-41110095 chr19:41111254-41111263 chr19:41110812-41110824 chr19:41110371-41110380 chr19:41112230-41112240 chr19:41111253-41111265 chr19:41109905-41109916 chr19:41108095-41108105 chr19:41112249-41112258 chr19:41109905-41109917 chr19:41112461-41112473 chr19:41110814-41110823 chr19:41111575-41111584 chr19:41110187-41110199 chr19:41110812-41110824 chr19:41109689-41109703 chr19:41110371-41110381 chr19:41109906-41109915 chr19:41110020-41110034
13	MXI1	chr19:41108742-41112633	SK-N-SH	brain:	n/a	chr19:41112101-41112110
14	TEAD4	chr19:41108953-41110362	K562	blood:	n/a	n/a
15	MAX	chr19:41106852-41112636	HCT-116	colon:	n/a	chr19:41108140-41108149 chr19:41106996-41107006 chr19:41109621-41109631 chr19:41107680-41107690 chr19:41110033-41110043 chr19:41112230-41112240 chr19:41108141-41108148 chr19:41109693-41109703 chr19:41110085-41110095 chr19:41107176-41107186 chr19:41108976-41108985
16	POLR2A	chr19:41107890-41109191	HCT-116	colon:	n/a	n/a
17	YY1	chr19:41108899-41109455	H1-hESC	embryonic stem cell:	n/a	n/a
18	STAT1	chr19:41108176-41110054	Hela-S3	cervix:	n/a	chr19:41109314-41109337 chr19:41109314-41109323 chr19:41109308-41109328 chr19:41109313-41109322 chr19:41108202-41108214 chr19:41109636-41109648 chr19:41109254-41109266 chr19:41109312-41109323 chr19:41109689-41109701 chr19:41108395-41108407 chr19:41109104-41109116 chr19:41109777-41109789 chr19:41109311-41109325
19	ZNF263	chr19:41107273-41112166	HEK293-T-REx	kidney:	n/a	chr19:41107583-41107592 chr19:41109635-41109644
20	CTCF	chr19:41108920-41109070	K562	blood:	n/a	n/a
21	POLR2A	chr19:41107198-41112648	SK-N-MC	brain:	n/a	n/a
22	BCL3	chr19:41107600-41112675	A549	lung:	n/a	chr19:41109906-41109915 chr19:41109623-41109636 chr19:41109787-41109796 chr19:41110189-41110198 chr19:41109814-41109827 chr19:41108090-41108099 chr19:41108193-41108202 chr19:41109619-41109632
23	CTCF	chr19:41107935-41108976	K562	blood:	n/a	chr19:41108676-41108684 chr19:41108186-41108199 chr19:41108187-41108196 chr19:41108671-41108689 chr19:41108181-41108199 chr19:41108183-41108196 chr19:41108666-41108687 chr19:41108184-41108194
24	CTCF	chr19:41108960-41109110	BE2_C	brain:	n/a	n/a
25	POLR2A	chr19:41106943-41109073	K562	blood:	n/a	n/a
26	NR2F2	chr19:41107695-41110916	K562	blood:	n/a	n/a
27	POLR2A	chr19:41107772-41110454	PFSK-1	brain:	n/a	n/a
28	ZBTB7A	chr19:41106872-41108999	K562	blood:	n/a	chr19:41107686-41107694 chr19:41107071-41107080 chr19:41108178-41108185 chr19:41108370-41108378 chr19:41108182-41108191
29	POLR2A	chr19:41107880-41109441	HUVEC	blood vessel:	n/a	n/a
30	MAZ	chr19:41106420-41110503	IMR90	lung:	n/a	chr19:41108140-41108149 chr19:41106996-41107006 chr19:41109621-41109631 chr19:41107680-41107690 chr19:41110033-41110043 chr19:41108141-41108148 chr19:41106647-41106657 chr19:41109693-41109703 chr19:41110085-41110095 chr19:41107176-41107186 chr19:41108976-41108985
31	POLR2A	chr19:41106762-41114701	K562	blood:	n/a	n/a
32	CTCF	chr19:41108880-41109030	AG04450	lung:	n/a	n/a
33	POLR2A	chr19:41107105-41114419	Hela-S3	cervix:	n/a	n/a
34	SIX5	chr19:41107632-41112495	A549	lung:	n/a	chr19:41110856-41110872
35	POLR2A	chr19:41108184-41110374	PBDE	blood:	n/a	n/a
36	ZBTB7A	chr19:41107389-41109264	K562	blood:	n/a	chr19:41107686-41107694 chr19:41108178-41108185 chr19:41108370-41108378 chr19:41108182-41108191

No.	Distal block	Cell Line	Cell type
1	chr19:41033096..41035483-chr19:41108426..41110262,2	MCF-7	breast:
2	chr19:41030467..41033307-chr19:41108722..41110398,2	MCF-7	breast:
3	chr19:40909995..40911526-chr19:41108177..41110853,2	K562	blood:
4	chr19:40967363..40973578-chr19:41101518..41109514,8	K562	blood:
5	chr19:40969243..40970765-chr19:41108513..41110039,2	MCF-7	breast:
6	chr19:41053869..41056282-chr19:41108308..41111059,2	MCF-7	breast:
7	chr19:41107019..41113650-chr19:41128672..41134191,9	K562	blood:
8	chr19:40931237..40933267-chr19:41108598..41112233,4	K562	blood:
9	chr19:41075066..41076899-chr19:41107772..41111753,3	K562	blood:
10	chr19:41035178..41037459-chr19:41108558..41111461,2	MCF-7	breast:
11	chr19:41108472..41109833-chr19:41140193..41141071,7	MCF-7	breast:
12	chr19:41031800..41040224-chr19:41101608..41111828,17	K562	blood:
13	chr19:41084714..41088277-chr19:41106890..41109795,3	K562	blood:
14	chr19:41031800..41041078-chr19:41106134..41114466,15	K562	blood:
15	chr19:41074602..41077015-chr19:41107246..41111753,6	K562	blood:
16	chr19:41108422..41113817-chr19:41128876..41134100,7	MCF-7	breast:
17	chr19:40970640..40973195-chr19:41107920..41111386,3	K562	blood:
18	chr19:41089494..41092756-chr19:41107049..41110047,4	K562	blood:
19	chr19:41107627..41110532-chr19:41140107..41142181,2	K562	blood:
20	chr19:41084483..41086767-chr19:41108737..41110541,2	MCF-7	breast:
21	chr19:41108549..41110281-chr19:41195453..41197402,2	MCF-7	breast:
22	chr19:41108277..41110183-chr19:41222910..41224615,2	MCF-7	breast:

Variant related genes	Relation type
LTBP4	TF binding region
ENSG00000105245	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000160460	Chromatin interaction
ENSG00000160410	Chromatin interaction
ENSG00000086544	Chromatin interaction
ENSG00000090013	Chromatin interaction
ENSG00000123815	Chromatin interaction
ENSG00000090006	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10402698	0.80[ASN][1000 genomes]
rs10403467	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10403833	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10403963	0.93[ASW][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.95[LWK][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.91[TSI][hapmap];0.91[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10405930	0.87[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1051303	1.00[CHB][hapmap];0.98[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11083561	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1131620	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11667706	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11667772	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12610819	0.83[CHB][hapmap];0.83[CHD][hapmap];0.80[GIH][hapmap]
rs12611045	0.96[ASN][1000 genomes]
rs12980111	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1318544	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1864074	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1864078	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1869712	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2278242	0.83[CHB][hapmap]
rs2278246	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2303727	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2303729	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.95[MEX][hapmap];0.82[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2369006	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs2604902	0.86[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.95[MEX][hapmap];0.96[MKK][hapmap];0.91[TSI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28649715	0.96[ASN][1000 genomes]
rs28655571	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs392726	0.94[CHB][hapmap];0.93[CHD][hapmap];0.84[TSI][hapmap];0.88[ASN][1000 genomes]
rs393569	0.94[CHB][hapmap];0.85[CHD][hapmap];0.84[TSI][hapmap];0.83[ASN][1000 genomes]
rs396118	0.87[ASN][1000 genomes]
rs404584	0.87[CHB][hapmap];0.84[ASN][1000 genomes]
rs406133	0.83[ASN][1000 genomes]
rs410101	0.83[CHB][hapmap];0.85[CHD][hapmap]
rs413901	0.83[CHB][hapmap];0.85[CHD][hapmap]
rs415075	0.84[ASN][1000 genomes]
rs420720	0.86[ASN][1000 genomes]
rs4803348	0.96[ASN][1000 genomes]
rs56353506	0.96[ASN][1000 genomes]
rs7171	0.88[ASN][1000 genomes]
rs7257696	0.81[CHD][hapmap]
rs7259067	0.94[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.86[TSI][hapmap];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7259237	1.00[CHB][hapmap];0.98[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.87[TSI][hapmap];0.97[ASN][1000 genomes]
rs7259554	1.00[CHB][hapmap];0.98[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.87[TSI][hapmap];0.97[ASN][1000 genomes]
rs8107014	1.00[CHB][hapmap];0.98[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs919307	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv911714	chr19:41006426-41165252	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv911715	chr19:41014922-41141434	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv1057634	chr19:41019512-41174259	Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv911716	chr19:41023511-41109456	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv911717	chr19:41023511-41141434	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS 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	33 gene(s)	inside rSNPs	diseases
7	nsv911719	chr19:41033109-41147087	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	nsv911720	chr19:41033109-41156940	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv911721	chr19:41040334-41124931	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic 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 lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv911722	chr19:41040334-41176403	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv911723	chr19:41075990-41195279	Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv869561	chr19:41077513-41139834	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv1064699	chr19:41086506-41174259	Genic enhancers Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
14	nsv911724	chr19:41089505-41165252	Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
15	nsv911725	chr19:41090190-41114065	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
16	nsv911726	chr19:41090190-41141434	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs10410606	ZNF155	cis	cerebellum	SCAN
rs10410606	CA11	cis	cerebellum	SCAN
rs10410606	ELSPBP1	cis	cerebellum	SCAN
rs10410606	B9D2	cis	parietal	SCAN
rs10410606	SHKBP1	cis	Whole Blood	GTEx
rs10410606	PGLYRP1	cis	cerebellum	SCAN
rs10410606	CEACAM6	cis	cerebellum	SCAN
rs10410606	GSK3A	cis	cerebellum	SCAN
rs10410606	ZNF296	cis	cerebellum	SCAN
rs10410606	SHKBP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41102400-41109200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
2	chr19:41105800-41109200	Enhancers	Fetal Heart	heart
3	chr19:41106000-41136800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:41106400-41109800	Active TSS	Aorta	Aorta
5	chr19:41107200-41110000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr19:41107400-41109000	Enhancers	Gastric	stomach
7	chr19:41107400-41109000	Flanking Active TSS	Right Ventricle	heart
8	chr19:41107400-41109400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr19:41107400-41109400	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr19:41107400-41109600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr19:41107400-41109600	Bivalent Enhancer	Fetal Thymus	thymus
12	chr19:41107400-41110200	Flanking Active TSS	NHLF	lung
13	chr19:41107400-41110400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
14	chr19:41107600-41109400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
15	chr19:41107600-41109600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr19:41107600-41109600	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr19:41107600-41109600	Enhancers	Pancreas	Pancrea
18	chr19:41107800-41109000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:41107800-41109000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
20	chr19:41107800-41109000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr19:41107800-41109200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr19:41107800-41109200	Enhancers	Lung	lung
23	chr19:41107800-41109200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr19:41107800-41109400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:41107800-41109400	Enhancers	Primary hematopoietic stem cells	blood
26	chr19:41107800-41109400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
27	chr19:41107800-41109400	Enhancers	Small Intestine	intestine
28	chr19:41107800-41109600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr19:41107800-41109600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr19:41107800-41109600	Enhancers	Brain Substantia Nigra	brain
31	chr19:41107800-41109600	Flanking Active TSS	Fetal Lung	lung
32	chr19:41107800-41109600	Flanking Active TSS	A549	lung
33	chr19:41108000-41109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr19:41108000-41109000	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr19:41108000-41109200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr19:41108000-41109200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr19:41108000-41109200	Weak transcription	GM12878-XiMat	blood
38	chr19:41108000-41109400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:41108000-41109400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr19:41108000-41109400	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr19:41108000-41109400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr19:41108000-41109400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr19:41108000-41109400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:41108000-41109600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr19:41108000-41109600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr19:41108000-41109600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:41108000-41109600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:41108000-41109600	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr19:41108000-41109600	Flanking Active TSS	NHEK	skin
50	chr19:41108000-41110400	Flanking Active TSS	Fetal Intestine Small	intestine

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