Variant report

Variant	rs1200151
Chromosome Location	chr1:169088455-169088456
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:169087143..169088781-chr1:169092217..169094524,2	K562	blood:
2	chr1:169087281..169089561-chr1:169092217..169094257,2	K562	blood:
3	chr1:169087780..169089721-chr1:169091214..169093379,2	MCF-7	breast:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1040502	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs10919064	0.98[ASN][1000 genomes]
rs1200150	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3753292	0.98[ASN][1000 genomes]
rs3766038	0.96[CEU][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3766039	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs754549	0.87[EUR][1000 genomes]
rs754550	0.88[EUR][1000 genomes]
rs754551	0.96[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv831858	chr1:169022383-169179068	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169079800-169094600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr1:169079800-169105800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr1:169080200-169088800	Genic enhancers	Hela-S3	cervix
4	chr1:169080200-169089800	Genic enhancers	Fetal Intestine Large	intestine
5	chr1:169081000-169098200	Weak transcription	Small Intestine	intestine
6	chr1:169081200-169091800	Strong transcription	Fetal Brain Female	brain
7	chr1:169082200-169097600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:169082400-169097400	Weak transcription	Fetal Thymus	thymus
9	chr1:169083400-169088600	Weak transcription	HSMMtube	muscle
10	chr1:169083400-169090400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr1:169083600-169094600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:169084000-169088800	Weak transcription	Ovary	ovary
13	chr1:169084000-169094000	Weak transcription	Primary T cells from cord blood	blood
14	chr1:169084200-169099200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:169084800-169089600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:169085000-169089600	Transcr. at gene 5' and 3'	A549	lung
17	chr1:169085400-169090800	Enhancers	NHLF	lung
18	chr1:169085400-169091000	Genic enhancers	HepG2	liver
19	chr1:169085400-169097600	Weak transcription	Fetal Brain Male	brain
20	chr1:169085400-169102200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:169085600-169088800	Weak transcription	K562	blood
22	chr1:169085600-169089200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:169085600-169090400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr1:169085600-169090800	Weak transcription	Lung	lung
25	chr1:169085600-169091000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:169085600-169091200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:169085600-169091800	Genic enhancers	Rectal Mucosa Donor 31	rectum
28	chr1:169085600-169092400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:169085600-169094800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr1:169085600-169096600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr1:169085800-169088600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:169085800-169088600	Weak transcription	Fetal Muscle Leg	muscle
33	chr1:169085800-169089200	Genic enhancers	Brain Anterior Caudate	brain
34	chr1:169085800-169089600	Weak transcription	Stomach Smooth Muscle	stomach
35	chr1:169085800-169089600	Enhancers	NHEK	skin
36	chr1:169085800-169090800	Weak transcription	Aorta	Aorta
37	chr1:169085800-169090800	Weak transcription	Spleen	Spleen
38	chr1:169085800-169091000	Weak transcription	Right Atrium	heart
39	chr1:169085800-169091400	Genic enhancers	Duodenum Mucosa	Duodenum
40	chr1:169085800-169094000	Weak transcription	Placenta	Placenta
41	chr1:169085800-169097400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:169085800-169100000	Weak transcription	Thymus	Thymus
43	chr1:169086000-169088600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:169086000-169088600	Weak transcription	Fetal Stomach	stomach
45	chr1:169086200-169094200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr1:169086200-169102000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:169086200-169102000	Weak transcription	GM12878-XiMat	blood
48	chr1:169086200-169102400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr1:169086400-169089600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:169086400-169089800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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