Variant report

Variant	rs7224335
Chromosome Location	chr17:17116544-17116545
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17116103..17119512-chr17:17125606..17128978,3	K562	blood:
2	chr17:17107906..17110805-chr17:17116134..17118817,2	K562	blood:
3	chr17:17115727..17117859-chr17:17118196..17119730,2	K562	blood:
4	chr17:17107906..17111698-chr17:17113566..17117634,4	K562	blood:
5	chr17:17115314..17118289-chr17:17131903..17134654,2	K562	blood:

Variant related genes	Relation type
ENSG00000154803	Chromatin interaction
ENSG00000179598	Chromatin interaction

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

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

rs_ID	r²[population]
rs12939385	1.00[CEU][hapmap]
rs16961495	1.00[CEU][hapmap]
rs7210263	1.00[CEU][hapmap]
rs7212534	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap]
rs7224474	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8068606	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs8077027	1.00[CEU][hapmap]
rs8077113	1.00[CEU][hapmap]
rs8082001	0.90[GIH][hapmap]

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	nsv833380	chr17:17088416-17241206	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1065811	chr17:17104760-17225204	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17109400-17120400	Weak transcription	Fetal Kidney	kidney
2	chr17:17109400-17131600	Weak transcription	Fetal Heart	heart
3	chr17:17109600-17118200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr17:17109600-17124200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr17:17109800-17116600	Weak transcription	HUVEC	blood vessel
6	chr17:17109800-17117200	Weak transcription	Psoas Muscle	Psoas
7	chr17:17109800-17123200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr17:17110000-17116600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr17:17110000-17121000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr17:17110200-17117000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr17:17110400-17116800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr17:17110400-17120400	Weak transcription	Hela-S3	cervix
13	chr17:17110800-17120000	Weak transcription	K562	blood
14	chr17:17111800-17120600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr17:17113200-17135200	Strong transcription	Fetal Intestine Small	intestine
16	chr17:17113200-17136600	Strong transcription	Fetal Stomach	stomach
17	chr17:17113400-17131400	Strong transcription	Brain Anterior Caudate	brain
18	chr17:17113400-17131400	Strong transcription	Brain Substantia Nigra	brain
19	chr17:17113400-17134600	Strong transcription	Fetal Muscle Trunk	muscle
20	chr17:17113400-17136200	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr17:17113800-17116800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr17:17113800-17134600	Strong transcription	Fetal Muscle Leg	muscle
23	chr17:17113800-17137600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr17:17114000-17122600	Strong transcription	A549	lung
25	chr17:17114000-17131200	Strong transcription	Liver	Liver
26	chr17:17114000-17131200	Strong transcription	Left Ventricle	heart
27	chr17:17114000-17134800	Strong transcription	Fetal Intestine Large	intestine
28	chr17:17114000-17135200	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr17:17114000-17136200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr17:17114000-17136200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr17:17114000-17136400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:17114000-17136400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr17:17114000-17136400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr17:17114000-17136400	Strong transcription	Placenta	Placenta
35	chr17:17114000-17136600	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr17:17114200-17131600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr17:17114200-17131600	Strong transcription	Spleen	Spleen
38	chr17:17114200-17136600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr17:17114400-17131400	Strong transcription	Lung	lung
40	chr17:17114400-17136200	Strong transcription	Primary T cells from cord blood	blood
41	chr17:17114400-17136200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:17114400-17136400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr17:17114400-17136600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr17:17114600-17116800	Strong transcription	Adipose Nuclei	Adipose
45	chr17:17114600-17121000	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr17:17114600-17121600	Strong transcription	Primary B cells from cord blood	blood
47	chr17:17114600-17134800	Strong transcription	Duodenum Mucosa	Duodenum
48	chr17:17114600-17136000	Strong transcription	Fetal Brain Female	brain
49	chr17:17114600-17136200	Strong transcription	NHLF	lung
50	chr17:17114600-17136400	Strong transcription	HUES6 Cell Line	embryonic stem cell

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