Variant report

Variant	rs73673806
Chromosome Location	chr7:7791569-7791570
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10156195	0.86[ASN][1000 genomes]
rs10281466	0.86[ASN][1000 genomes]
rs17137236	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73673805	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv606042	chr7:7427535-7876466	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv887477	chr7:7531819-7810122	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1032670	chr7:7535515-8017077	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv8043	chr7:7589195-7862802	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv887478	chr7:7670718-7917360	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv887480	chr7:7681131-7917360	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv887483	chr7:7682439-7798217	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv887485	chr7:7692483-7917360	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv2752177	chr7:7729247-8177689	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv1026564	chr7:7734846-7897847	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv887487	chr7:7740914-7802561	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	nsv887488	chr7:7770203-7794484	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv887489	chr7:7770203-7913311	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7773000-7802000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:7778600-7797400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:7779800-7796000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:7779800-7800200	Weak transcription	Thymus	Thymus
5	chr7:7785600-7800800	Weak transcription	Primary B cells from cord blood	blood
6	chr7:7786400-7800200	Weak transcription	Fetal Thymus	thymus
7	chr7:7789800-7791600	Enhancers	Colon Smooth Muscle	Colon
8	chr7:7790200-7791800	Enhancers	HepG2	liver
9	chr7:7790400-7791600	Active TSS	Stomach Smooth Muscle	stomach
10	chr7:7790400-7801400	Weak transcription	Stomach Mucosa	stomach
11	chr7:7790600-7791600	Enhancers	Adipose Nuclei	Adipose
12	chr7:7790600-7791600	Flanking Active TSS	Liver	Liver
13	chr7:7790800-7791600	Enhancers	Fetal Heart	heart
14	chr7:7790800-7791600	Enhancers	Hela-S3	cervix
15	chr7:7791000-7791600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:7791000-7791600	Enhancers	Fetal Intestine Small	intestine
17	chr7:7791000-7791600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr7:7791000-7791600	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr7:7791000-7795200	Weak transcription	Brain Substantia Nigra	brain
20	chr7:7791000-7801400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:7791200-7791600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr7:7791200-7791600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr7:7791200-7791600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:7791200-7791600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:7791200-7791600	Active TSS	Duodenum Mucosa	Duodenum
26	chr7:7791200-7791600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr7:7791200-7791600	Enhancers	Fetal Intestine Large	intestine
28	chr7:7791200-7791600	Enhancers	Fetal Muscle Leg	muscle
29	chr7:7791200-7791600	Enhancers	Placenta	Placenta
30	chr7:7791200-7791600	Enhancers	Fetal Stomach	stomach
31	chr7:7791200-7791600	Enhancers	Psoas Muscle	Psoas
32	chr7:7791200-7791600	Flanking Active TSS	Rectal Smooth Muscle	rectum
33	chr7:7791200-7791800	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr7:7791200-7794400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:7791400-7791600	Weak transcription	Esophagus	oesophagus

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