Variant report

Variant	rs11857291
Chromosome Location	chr15:78219757-78219758
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78219748-78219798	NH-A	brain:	n/a
2	chr15:78219748-78219798	AoSMC	blood vessel:	n/a
3	chr15:78219748-78219798	GM12891	blood:	n/a
4	chr15:78219748-78219798	HL-60	blood:	n/a
5	chr15:78219748-78219798	HUVEC	blood vessel:	n/a
6	chr15:78219748-78219798	AG09319	gingival:	n/a
7	chr15:78219748-78219798	HRE	kidney:	n/a
8	chr15:78219748-78219798	HCM	heart:	n/a
9	chr15:78219748-78219798	HAEpiC	amniotic membrane:	n/a
10	chr15:78219748-78219798	K562	blood:	n/a
11	chr15:78219748-78219798	HCF	heart:	n/a
12	chr15:78219748-78219798	SK-N-MC	brain:	n/a
13	chr15:78219748-78219798	MCF-7	breast:	n/a
14	chr15:78219748-78219798	HCT-116	colon:	n/a
15	chr15:78219748-78219798	GM06990	blood:	n/a
16	chr15:78219748-78219798	GM12878	blood:	n/a
17	chr15:78219748-78219798	BJ	skin:	n/a
18	chr15:78219748-78219798	T-47D	breast:	n/a
19	chr15:78219748-78219798	PFSK-1	brain:	n/a
20	chr15:78219748-78219798	HepG2	liver:	n/a
21	chr15:78219748-78219798	HEEpiC	esophagus:	n/a
22	chr15:78219748-78219798	AG09309	skin:	n/a
23	chr15:78219748-78219798	AG04449	skin:	fetal
24	chr15:78219748-78219798	U87	brain:	n/a
25	chr15:78219748-78219798	Hepatocyte	liver:	n/a
26	chr15:78219748-78219798	HNPCEpiC	eye:	n/a
27	chr15:78219748-78219798	ProgFib	skin:	n/a
28	chr15:78219748-78219798	SK-N-SH_RA	brain:	n/a
29	chr15:78219748-78219798	AG10803	skin:	n/a
30	chr15:78219748-78219798	GM19239	blood:	n/a
31	chr15:78219748-78219798	PANC-1	pancreas:	n/a
32	chr15:78219748-78219798	Hela-S3	cervix:	n/a
33	chr15:78219748-78219798	PrEC	prostate:	n/a
34	chr15:78219748-78219798	BE2_C	brain:	n/a
35	chr15:78219748-78219798	HRPEpiC	eye:	n/a
36	chr15:78219748-78219798	HMEC	breast:	n/a
37	chr15:78219748-78219798	GM12892	blood:	n/a
38	chr15:78219748-78219798	SKMC	muscle:	n/a
39	chr15:78219748-78219798	Jurkat	blood:	n/a
40	chr15:78219748-78219798	NHBE	bronchial:	n/a
41	chr15:78219748-78219798	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:78219748-78219798	NB4	blood:	n/a
43	chr15:78219748-78219798	SAEC	small airway:	n/a
44	chr15:78219748-78219798	HRCEpiC	kidney:	n/a
45	chr15:78219748-78219798	HCPEpiC	choroid plexus:	n/a
46	chr15:78219748-78219798	LNCaP	prostate:	n/a
47	chr15:78219748-78219798	A549	lung:	n/a
48	chr15:78219748-78219798	HIPEpiC	eye:	n/a
49	chr15:78219748-78219798	NT2-D1	testis:	n/a
50	chr15:78219748-78219798	MCF10A-Er-Src	breast:	n/a

No data

Variant related genes	Relation type
ENSG00000260776	CpG island

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11072702	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11633345	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11638015	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12148340	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12148737	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12899553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12904130	0.82[EUR][1000 genomes]
rs12904447	0.81[AMR][1000 genomes]
rs12907928	0.81[AMR][1000 genomes]
rs12908616	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12908664	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12913714	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12914021	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12915431	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2004373	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34028432	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35093138	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4073671	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4243067	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4243068	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4366682	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4435228	0.81[EUR][1000 genomes]
rs4530095	0.82[EUR][1000 genomes]
rs4605126	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4886543	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4886966	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4886968	0.82[EUR][1000 genomes]
rs4886969	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4886971	0.84[EUR][1000 genomes]
rs4886973	0.83[EUR][1000 genomes]
rs55849958	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60003906	0.81[AMR][1000 genomes]
rs67630434	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71400918	0.81[EUR][1000 genomes]
rs71400932	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71400933	0.82[ASN][1000 genomes]
rs7174328	0.82[ASN][1000 genomes]
rs72732507	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72732509	0.80[EUR][1000 genomes]
rs72732511	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73456876	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1833316	chr15:78081307-78328108	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv904426	chr15:78090630-78264164	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv904427	chr15:78129964-78251431	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv976954	chr15:78153346-78255825	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1046383	chr15:78153850-78229596	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv904428	chr15:78156238-78230906	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv904429	chr15:78160362-78251431	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	esv1823600	chr15:78200594-78219757	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	esv18540	chr15:78202973-78227329	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv9281	chr15:78213140-78225495	Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78203200-78220200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr15:78203200-78227400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78219000-78222800	Weak transcription	HepG2	liver
4	chr15:78219200-78222600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr15:78219200-78228200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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