Variant report

Variant	rs73485799
Chromosome Location	chr7:140233427-140233428
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	chr7:140177793..140180325-chr7:140232986..140234950,2	K562	blood:
2	chr7:140233192..140234849-chr7:140239387..140241238,2	K562	blood:

Variant related genes	Relation type
ENSG00000133606	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11771129	1.00[AMR][1000 genomes]
rs73483934	0.80[AFR][1000 genomes]
rs73483942	0.80[AFR][1000 genomes]
rs73487622	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73487670	0.80[AFR][1000 genomes]
rs73491542	0.80[AFR][1000 genomes]
rs73491556	0.80[AFR][1000 genomes]
rs73491570	0.80[AFR][1000 genomes]
rs73491576	0.80[AFR][1000 genomes]
rs73502435	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803443	chr7:140146694-140263109	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2761112	chr7:140191538-140234571	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv464735	chr7:140195463-140233585	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv608501	chr7:140195463-140233585	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	nsv1015856	chr7:140197079-140235677	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv1019815	chr7:140206590-140235677	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	esv1802929	chr7:140212566-140285491	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140207000-140241000	Weak transcription	Fetal Brain Male	brain
2	chr7:140218200-140241400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:140219200-140240800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:140219600-140240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:140222000-140234600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:140223400-140241000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:140223600-140235000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:140223600-140238000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:140223600-140240800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:140223800-140234400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr7:140224000-140239200	Weak transcription	Brain Anterior Caudate	brain
12	chr7:140226000-140241000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr7:140226000-140241400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr7:140226000-140244000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:140226000-140244000	Weak transcription	Pancreas	Pancrea
16	chr7:140226200-140241000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:140226200-140262800	Weak transcription	Gastric	stomach
18	chr7:140226400-140237200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:140226400-140239200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:140226600-140240200	Weak transcription	Right Ventricle	heart
21	chr7:140226600-140241200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:140226600-140241400	Weak transcription	Fetal Intestine Large	intestine
23	chr7:140226800-140239000	Weak transcription	Fetal Kidney	kidney
24	chr7:140226800-140240800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr7:140227000-140238800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:140227200-140234600	Weak transcription	Spleen	Spleen
27	chr7:140227200-140239400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:140227400-140239200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:140227400-140241000	Weak transcription	Right Atrium	heart
30	chr7:140227600-140237600	Weak transcription	Stomach Smooth Muscle	stomach
31	chr7:140227600-140240800	Weak transcription	NH-A	brain
32	chr7:140227600-140243800	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:140228200-140244000	Weak transcription	Brain Substantia Nigra	brain
34	chr7:140229800-140241000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:140230000-140234400	Weak transcription	Colon Smooth Muscle	Colon
36	chr7:140230400-140240800	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr7:140230600-140234200	Weak transcription	Fetal Lung	lung
38	chr7:140230600-140234600	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr7:140230600-140240000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:140232200-140240800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:140232400-140233600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr7:140232400-140233600	Strong transcription	Fetal Intestine Small	intestine
43	chr7:140232400-140233600	Strong transcription	Left Ventricle	heart
44	chr7:140232400-140234400	Strong transcription	Fetal Brain Female	brain
45	chr7:140233000-140233600	Strong transcription	Brain Germinal Matrix	brain
46	chr7:140233000-140234400	Weak transcription	Psoas Muscle	Psoas
47	chr7:140233000-140235200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:140233000-140235400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:140233000-140240800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:140233200-140233600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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