Variant report

Variant	rs7206995
Chromosome Location	chr17:38306365-38306366
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:38296494..38299896-chr17:38301046..38306469,5	MCF-7	breast:
2	chr17:38295543..38297731-chr17:38305864..38307419,2	K562	blood:

Variant related genes	Relation type
ENSG00000108349	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs28410661	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28750099	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9896339	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9903261	0.91[ASW][hapmap];0.83[MKK][hapmap]
rs9904120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9906274	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs9909548	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9910546	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9911936	1.00[ASW][hapmap];0.89[LWK][hapmap];0.91[MKK][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833444	chr17:38242823-38437280	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv525796	chr17:38306365-38405037	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38297600-38306600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr17:38297600-38313400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr17:38297600-38318200	Weak transcription	Aorta	Aorta
4	chr17:38297600-38318200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr17:38297600-38325200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr17:38297800-38309400	Weak transcription	Right Ventricle	heart
7	chr17:38297800-38318400	Weak transcription	Stomach Mucosa	stomach
8	chr17:38297800-38333000	Strong transcription	Fetal Muscle Trunk	muscle
9	chr17:38297800-38336600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr17:38298000-38310800	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr17:38298000-38311800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr17:38298000-38324200	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr17:38298000-38330400	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr17:38298000-38330800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:38298200-38306400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr17:38298200-38307400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:38298200-38307600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr17:38298200-38308400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr17:38298200-38313000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr17:38298200-38313600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr17:38298200-38318000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr17:38298200-38318200	Weak transcription	Small Intestine	intestine
23	chr17:38298200-38324200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr17:38298200-38324400	Strong transcription	Fetal Stomach	stomach
25	chr17:38298200-38333000	Strong transcription	Fetal Thymus	thymus
26	chr17:38298400-38307000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr17:38298400-38324200	Weak transcription	Fetal Heart	heart
28	chr17:38298600-38307000	Strong transcription	Brain Anterior Caudate	brain
29	chr17:38298600-38309400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr17:38298600-38310600	Strong transcription	Lung	lung
31	chr17:38298600-38316400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr17:38298600-38319600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr17:38298600-38332200	Strong transcription	Fetal Intestine Small	intestine
34	chr17:38298800-38306400	Weak transcription	NHLF	lung
35	chr17:38298800-38313200	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr17:38298800-38314000	Strong transcription	Fetal Muscle Leg	muscle
37	chr17:38299200-38319600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr17:38300000-38310200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr17:38300000-38312200	Strong transcription	Fetal Intestine Large	intestine
40	chr17:38300600-38306400	Weak transcription	Right Atrium	heart
41	chr17:38301400-38313400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr17:38301600-38307400	Strong transcription	Primary hematopoietic stem cells	blood
43	chr17:38301600-38308400	Strong transcription	A549	lung
44	chr17:38301600-38324200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr17:38301800-38306800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr17:38301800-38307600	Strong transcription	HSMM	muscle
47	chr17:38301800-38309800	Strong transcription	Fetal Brain Female	brain
48	chr17:38301800-38313200	Strong transcription	Placenta	Placenta
49	chr17:38301800-38313200	Strong transcription	Osteobl	bone
50	chr17:38301800-38324200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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