Variant report

Variant	rs8192726
Chromosome Location	chr19:41354496-41354497
allele	G/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	RAD21	chr19:41354407-41354746	H1-hESC	embryonic stem cell:	n/a	chr19:41354700-41354710
2	CTCF	chr19:41354440-41354590	HEK293	kidney:	n/a	n/a
3	CTCF	chr19:41354345-41354814	H1-hESC	embryonic stem cell:	n/a	chr19:41354699-41354709
4	E2F6	chr19:41354442-41354867	H1-hESC	embryonic stem cell:	n/a	chr19:41354704-41354714 chr19:41354488-41354498
5	CTCF	chr19:41354460-41354610	AG10803	skin:	n/a	n/a
6	RAD21	chr19:41354430-41354753	H1-hESC	embryonic stem cell:	n/a	chr19:41354700-41354710
7	CTCF	chr19:41354435-41354719	H1-hESC	embryonic stem cell:	n/a	chr19:41354699-41354709
8	TCF12	chr19:41354423-41355199	A549	lung:	n/a	chr19:41354704-41354714
9	POLR2A	chr19:41354134-41354798	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr19:41354459-41354759	K562	blood:	n/a	chr19:41354699-41354709
11	FOSL2	chr19:41354343-41355071	A549	lung:	n/a	chr19:41354817-41354829
12	POLR2A	chr19:41354431-41354731	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr19:41354483-41354696	A549	lung:	n/a	n/a
14	GABPA	chr19:41354404-41354743	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr19:41354312-41354785	K562	blood:	n/a	chr19:41354699-41354709
16	CTCF	chr19:41354333-41354798	H1-hESC	embryonic stem cell:	n/a	chr19:41354699-41354709
17	TEAD4	chr19:41354182-41354846	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:41354480-41354686	Pancreas_OC	pancreas:	n/a	n/a
19	MAX	chr19:41354446-41354860	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr19:41354460-41354610	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr19:41354359-41354806	A549	lung:	n/a	chr19:41354699-41354709
22	RAD21	chr19:41354445-41354923	A549	lung:	n/a	chr19:41354700-41354710
23	MAX	chr19:41354436-41355056	A549	lung:	n/a	n/a
24	CTCF	chr19:41354322-41355358	A549	lung:	n/a	chr19:41355271-41355289 chr19:41354699-41354709
25	EGR1	chr19:41354400-41354689	H1-hESC	embryonic stem cell:	n/a	chr19:41354488-41354501 chr19:41354488-41354501 chr19:41354488-41354501 chr19:41354483-41354505
26	YY1	chr19:41354471-41355106	A549	lung:	n/a	chr19:41354491-41354505
27	YY1	chr19:41354385-41354815	H1-hESC	embryonic stem cell:	n/a	chr19:41354491-41354505
28	POLR2A	chr19:41354226-41354680	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:41354480-41354630	HFF	foreskin:	n/a	n/a
30	RAD21	chr19:41354320-41354874	H1-hESC	embryonic stem cell:	n/a	chr19:41354700-41354710 chr19:41354353-41354363
31	CTCF	chr19:41354437-41354750	K562	blood:	n/a	chr19:41354699-41354709
32	CTCF	chr19:41354460-41354610	HRE	kidney:	n/a	n/a
33	CTCF	chr19:41354442-41354722	A549	lung:	n/a	chr19:41354699-41354709
34	CTCF	chr19:41354488-41354703	IMR90	lung:	n/a	n/a
35	CTCF	chr19:41354480-41354630	AG04450	lung:	n/a	n/a
36	POLR2A	chr19:41354401-41354695	H1-hESC	embryonic stem cell:	n/a	n/a
37	E2F6	chr19:41354277-41354865	H1-hESC	embryonic stem cell:	n/a	chr19:41354704-41354714 chr19:41354488-41354498 chr19:41354415-41354422
38	CTCF	chr19:41354302-41354800	A549	lung:	n/a	chr19:41354699-41354709
39	CTCF	chr19:41354461-41354702	A549	lung:	n/a	n/a
40	RAD21	chr19:41354420-41354876	A549	lung:	n/a	chr19:41354700-41354710
41	MAX	chr19:41354429-41354858	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
CYP2A6	TF binding region

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs28399433	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:118 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758500	chr19:41291627-41546068	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2758762	chr19:41291627-41546068	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1066637	chr19:41309211-41597896	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv911729	chr19:41321372-41383828	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv2760509	chr19:41325004-41394336	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv1056244	chr19:41329218-41397661	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	esv1827726	chr19:41329872-41395056	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv1832156	chr19:41332004-41399077	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv817836	chr19:41333284-41363765	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1058732	chr19:41334726-41368987	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv1058747	chr19:41334726-41376007	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	esv2763010	chr19:41334738-41380946	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	esv14395	chr19:41337301-41393256	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	nsv9729	chr19:41337805-41394407	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv911730	chr19:41337923-41356054	Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv911731	chr19:41337923-41356751	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	nsv911732	chr19:41337923-41372475	Strong transcription Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv911733	chr19:41337923-41383828	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv911734	chr19:41337923-41392885	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
20	esv1830996	chr19:41338610-41391238	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
21	esv1832383	chr19:41338610-41393111	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
22	nsv1057349	chr19:41338835-41368987	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	nsv1062369	chr19:41338835-41369393	Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv1055204	chr19:41338835-41369697	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
25	nsv1063224	chr19:41338835-41370781	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv1055758	chr19:41338835-41370835	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
27	nsv1063909	chr19:41338835-41370933	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
28	nsv1066061	chr19:41338835-41376007	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
29	nsv1057452	chr19:41338835-41380934	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
30	nsv1057412	chr19:41339857-41368987	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
31	nsv1066701	chr19:41339857-41369697	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
32	nsv1066884	chr19:41339857-41370835	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
33	nsv1064519	chr19:41339857-41375954	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
34	nsv1059038	chr19:41339857-41380934	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
35	nsv1065886	chr19:41339857-41397661	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
36	esv33053	chr19:41340629-41400635	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
37	nsv911735	chr19:41341589-41356054	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
38	nsv911736	chr19:41341589-41356751	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
39	nsv516972	chr19:41341589-41363765	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
40	nsv579525	chr19:41341589-41372475	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
41	nsv911737	chr19:41341589-41372475	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
42	nsv911738	chr19:41341589-41379148	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
43	nsv911740	chr19:41341589-41383799	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
44	nsv911739	chr19:41341589-41383828	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
45	esv3335352	chr19:41345075-41375737	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
46	nsv1062605	chr19:41345146-41368987	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
47	nsv1062739	chr19:41345146-41369697	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
48	nsv1058924	chr19:41345146-41370933	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
49	nsv1067231	chr19:41345146-41380934	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
50	esv3584737	chr19:41345158-41380946	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41351000-41354600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr19:41353600-41354800	Enhancers	Lung	lung
3	chr19:41353800-41354800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
4	chr19:41354000-41354800	Enhancers	Spleen	Spleen
5	chr19:41354200-41354600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:41354200-41354600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:41354200-41354600	Flanking Active TSS	Liver	Liver
8	chr19:41354200-41354800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
9	chr19:41354200-41354800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr19:41354200-41354800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
11	chr19:41354200-41354800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr19:41354200-41355000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
13	chr19:41354200-41355000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr19:41354400-41354600	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
15	chr19:41354400-41354600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr19:41354400-41354600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr19:41354400-41354600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:41354400-41354600	Bivalent Enhancer	Fetal Brain Male	brain
19	chr19:41354400-41354600	Flanking Active TSS	Ovary	ovary
20	chr19:41354400-41354600	Enhancers	Rectal Smooth Muscle	rectum
21	chr19:41354400-41354600	Enhancers	Right Ventricle	heart
22	chr19:41354400-41354600	Bivalent Enhancer	Stomach Mucosa	stomach
23	chr19:41354400-41354800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
24	chr19:41354400-41354800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr19:41354400-41354800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:41354400-41354800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
27	chr19:41354400-41354800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr19:41354400-41354800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr19:41354400-41354800	Active TSS	Brain Angular Gyrus	brain
30	chr19:41354400-41354800	Enhancers	Brain Hippocampus Middle	brain
31	chr19:41354400-41354800	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr19:41354400-41354800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr19:41354400-41354800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr19:41354400-41354800	Enhancers	Gastric	stomach
35	chr19:41354400-41354800	Enhancers	Pancreas	Pancrea
36	chr19:41354400-41354800	Enhancers	Right Atrium	heart
37	chr19:41354400-41355000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
38	chr19:41354400-41355000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr19:41354400-41355000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:41354400-41355000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:41354400-41355000	Enhancers	Adipose Nuclei	Adipose
42	chr19:41354400-41355000	Bivalent/Poised TSS	A549	lung
43	chr19:41354400-41355200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr19:41354400-41355200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr19:41354400-41355200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr19:41354400-41355400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr19:41354400-41355600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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