Variant report

Variant	rs17169449
Chromosome Location	chr7:137612488-137612489
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	chr7:137611854..137613484-chr7:137685563..137687785,2	K562	blood:
2	chr7:137611909..137614588-chr7:137616790..137618864,2	K562	blood:

Variant related genes	Relation type
ENSG00000182158	Chromatin interaction
ENSG00000122787	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11763953	0.95[EUR][1000 genomes]
rs1871214	0.82[CEU][hapmap]
rs28663485	0.95[EUR][1000 genomes]
rs57385695	0.95[EUR][1000 genomes]
rs724064	0.82[CEU][hapmap]
rs7808800	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv831150	chr7:137500559-137652808	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv518070	chr7:137534627-137808839	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv5964	chr7:137599451-137616300	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 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	chr7:137588800-137615400	Weak transcription	Stomach Mucosa	stomach
2	chr7:137588800-137618400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr7:137588800-137620200	Weak transcription	Dnd41	blood
4	chr7:137589600-137613600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr7:137592400-137615000	Weak transcription	Hela-S3	cervix
6	chr7:137594600-137618000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:137598800-137617000	Weak transcription	Small Intestine	intestine
8	chr7:137599800-137614800	Weak transcription	HMEC	breast
9	chr7:137600200-137618400	Weak transcription	Fetal Thymus	thymus
10	chr7:137600800-137612600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr7:137602600-137612600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr7:137603200-137617600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:137604600-137613000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:137605000-137614000	Strong transcription	Fetal Intestine Large	intestine
15	chr7:137605200-137618000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:137605400-137615200	Weak transcription	Pancreas	Pancrea
17	chr7:137605800-137618400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:137606400-137613400	Weak transcription	Psoas Muscle	Psoas
19	chr7:137606400-137619000	Weak transcription	Primary T cells from cord blood	blood
20	chr7:137606600-137617600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:137606600-137617600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:137606800-137614000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:137606800-137615000	Weak transcription	HUVEC	blood vessel
24	chr7:137606800-137615200	Weak transcription	Right Atrium	heart
25	chr7:137607400-137613200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr7:137607600-137614000	Strong transcription	Primary hematopoietic stem cells	blood
27	chr7:137607800-137613200	Strong transcription	Placenta	Placenta
28	chr7:137607800-137614400	Strong transcription	HepG2	liver
29	chr7:137608000-137613200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr7:137608000-137613200	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:137608000-137613200	Strong transcription	Primary B cells from cord blood	blood
32	chr7:137608000-137613400	Strong transcription	Adipose Nuclei	Adipose
33	chr7:137608000-137613800	Strong transcription	Liver	Liver
34	chr7:137608000-137613800	Strong transcription	Duodenum Mucosa	Duodenum
35	chr7:137608200-137613000	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr7:137608200-137613000	Strong transcription	Stomach Smooth Muscle	stomach
37	chr7:137608200-137613200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:137608200-137613200	Strong transcription	Fetal Muscle Trunk	muscle
39	chr7:137608200-137613200	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr7:137608200-137613600	Strong transcription	Fetal Muscle Leg	muscle
41	chr7:137608400-137613600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:137608400-137614200	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr7:137608600-137613000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:137608600-137613600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:137609000-137612600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr7:137609000-137613000	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr7:137609200-137613200	Strong transcription	NH-A	brain
48	chr7:137609400-137614200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr7:137609800-137613000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr7:137609800-137613000	Strong transcription	Rectal Mucosa Donor 31	rectum

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