Variant report

Variant	rs34695955
Chromosome Location	chr17:37808759-37808760
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	GATA3	chr17:37808476-37808841	T-47D	breast:	n/a	n/a
2	FOXA1	chr17:37808438-37808771	T-47D	breast:	n/a	chr17:37808661-37808676
3	TEAD4	chr17:37808593-37809426	HepG2	liver:	n/a	n/a
4	GATA3	chr17:37808431-37808836	T-47D	breast:	n/a	n/a
5	FOXA1	chr17:37808464-37808854	T-47D	breast:	n/a	chr17:37808661-37808676

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:37806774..37809121-chr17:37895420..37897002,2	MCF-7	breast:
2	chr17:37792000..37794042-chr17:37806624..37808948,2	MCF-7	breast:

Variant related genes	Relation type
STARD3	TF binding region
ENSG00000141738	Chromatin interaction
ENSG00000131748	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12103674	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs33938012	0.98[AFR][1000 genomes]
rs33978574	0.90[AFR][1000 genomes]
rs66482609	0.84[AFR][1000 genomes]
rs734645	0.97[AFR][1000 genomes]
rs9899653	0.85[AFR][1000 genomes]
rs9907501	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
10	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
11	esv1792029	chr17:37797757-37886460	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription 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 miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv908213	chr17:37807698-37839493	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37795000-37814000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr17:37795000-37823800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr17:37795200-37814000	Weak transcription	Aorta	Aorta
4	chr17:37795200-37814600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr17:37795400-37818000	Weak transcription	Fetal Kidney	kidney
6	chr17:37796400-37810000	Weak transcription	Colon Smooth Muscle	Colon
7	chr17:37796400-37810800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr17:37796600-37809800	Weak transcription	Dnd41	blood
9	chr17:37797000-37808800	Weak transcription	Brain Germinal Matrix	brain
10	chr17:37798200-37813800	Weak transcription	GM12878-XiMat	blood
11	chr17:37798800-37808800	Weak transcription	Ovary	ovary
12	chr17:37798800-37810400	Weak transcription	Fetal Thymus	thymus
13	chr17:37799800-37809400	Weak transcription	Liver	Liver
14	chr17:37799800-37812400	Weak transcription	Psoas Muscle	Psoas
15	chr17:37799800-37819600	Weak transcription	Osteobl	bone
16	chr17:37800000-37809400	Weak transcription	Adipose Nuclei	Adipose
17	chr17:37800000-37809400	Weak transcription	Esophagus	oesophagus
18	chr17:37800000-37809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr17:37800000-37810000	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr17:37800000-37812800	Weak transcription	NHLF	lung
21	chr17:37800000-37814000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr17:37800000-37815200	Weak transcription	HUVEC	blood vessel
23	chr17:37800000-37818600	Weak transcription	Hela-S3	cervix
24	chr17:37800000-37820000	Weak transcription	NH-A	brain
25	chr17:37800200-37809200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr17:37800200-37810000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr17:37800200-37810600	Enhancers	Fetal Brain Male	brain
28	chr17:37800200-37810600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr17:37800200-37816800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr17:37800400-37814000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr17:37800600-37816200	Weak transcription	NHEK	skin
32	chr17:37800800-37810000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr17:37801000-37814600	Weak transcription	Primary B cells from cord blood	blood
34	chr17:37801200-37809800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr17:37801400-37809400	Weak transcription	Right Atrium	heart
36	chr17:37801600-37808800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr17:37801600-37809000	Weak transcription	Fetal Muscle Leg	muscle
38	chr17:37801600-37809600	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr17:37801800-37817000	Weak transcription	A549	lung
40	chr17:37803000-37809800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr17:37803400-37814200	Strong transcription	Thymus	Thymus
42	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr17:37804000-37812600	Weak transcription	Rectal Smooth Muscle	rectum
44	chr17:37805400-37809800	Weak transcription	Primary B cells from peripheral blood	blood
45	chr17:37805600-37808800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr17:37806000-37810200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr17:37806400-37809000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr17:37806400-37809800	Enhancers	Lung	lung
49	chr17:37806400-37810200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr17:37806800-37808800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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