Variant report

Variant	rs28495349
Chromosome Location	chr8:103086081-103086082
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:103077871..103079434-chr8:103084965..103087880,2	K562	blood:
2	chr8:103084929..103087953-chr8:103089291..103092188,3	MCF-7	breast:
3	chr8:103084257..103086284-chr8:103112303..103114668,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10086088	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10090764	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10110783	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10955279	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11775854	0.96[EUR][1000 genomes]
rs11784583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11784616	0.96[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11785772	1.00[ASN][1000 genomes]
rs16869009	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17415172	0.88[ASN][1000 genomes]
rs56162098	0.98[EUR][1000 genomes]
rs56224216	0.93[AFR][1000 genomes]
rs56844350	0.85[AFR][1000 genomes]
rs62523038	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62523039	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6992873	0.93[AFR][1000 genomes]
rs6993476	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7012174	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7831372	0.84[ASN][1000 genomes]
rs7837308	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831411	chr8:102937991-103108140	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv891232	chr8:103001914-103138045	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv891233	chr8:103001914-103162638	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
4	nsv891234	chr8:103020391-103113701	Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv891235	chr8:103032394-103162638	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	nsv891237	chr8:103039917-103113701	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv891238	chr8:103055520-103116959	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv891239	chr8:103056517-103162638	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv891240	chr8:103070301-103162638	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
10	esv2754264	chr8:103070824-103170824	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
11	nsv891241	chr8:103079505-103162638	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103076600-103088800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:103076600-103089200	Weak transcription	NHDF-Ad	bronchial
3	chr8:103077000-103090400	Weak transcription	Aorta	Aorta
4	chr8:103080400-103088000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr8:103080600-103091400	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:103080800-103091200	Weak transcription	Psoas Muscle	Psoas
7	chr8:103080800-103092800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr8:103081000-103087000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr8:103082400-103090200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:103083400-103086800	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:103083400-103089000	Weak transcription	Ovary	ovary
12	chr8:103083400-103091200	Weak transcription	Left Ventricle	heart
13	chr8:103083600-103091400	Weak transcription	Fetal Brain Female	brain
14	chr8:103084000-103086400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr8:103084800-103092600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr8:103085000-103092400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:103085400-103086400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr8:103085800-103086600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr8:103085800-103087200	Enhancers	Primary T cells from cord blood	blood
20	chr8:103085800-103087400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr8:103086000-103087200	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr8:103086000-103087400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr8:103086000-103087400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr8:103086000-103087400	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr8:103086000-103087600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr8:103086000-103087600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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