Variant report

Variant	rs73673632
Chromosome Location	chr7:3632729-3632730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs17133456	1.00[EUR][1000 genomes]
rs17133464	1.00[EUR][1000 genomes]
rs17133467	1.00[EUR][1000 genomes]
rs17133471	1.00[EUR][1000 genomes]
rs17133477	1.00[EUR][1000 genomes]
rs17133479	1.00[EUR][1000 genomes]
rs17133481	1.00[EUR][1000 genomes]
rs55998900	1.00[EUR][1000 genomes]
rs56098725	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56114690	1.00[EUR][1000 genomes]
rs56862729	1.00[EUR][1000 genomes]
rs56938545	1.00[EUR][1000 genomes]
rs57075167	1.00[EUR][1000 genomes]
rs57546275	1.00[EUR][1000 genomes]
rs57628119	1.00[EUR][1000 genomes]
rs57785562	1.00[EUR][1000 genomes]
rs57815878	1.00[EUR][1000 genomes]
rs58061781	1.00[EUR][1000 genomes]
rs58504043	1.00[EUR][1000 genomes]
rs58540106	1.00[EUR][1000 genomes]
rs59206202	1.00[EUR][1000 genomes]
rs59932157	1.00[EUR][1000 genomes]
rs60080946	1.00[EUR][1000 genomes]
rs60091839	1.00[EUR][1000 genomes]
rs60207294	1.00[EUR][1000 genomes]
rs60660116	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61378554	1.00[EUR][1000 genomes]
rs73293539	1.00[EUR][1000 genomes]
rs73300296	1.00[EUR][1000 genomes]
rs73302261	1.00[EUR][1000 genomes]
rs73671845	1.00[EUR][1000 genomes]
rs73671852	1.00[EUR][1000 genomes]
rs73671853	1.00[EUR][1000 genomes]
rs73671863	1.00[EUR][1000 genomes]
rs73671864	1.00[EUR][1000 genomes]
rs73671879	1.00[EUR][1000 genomes]
rs73671888	1.00[EUR][1000 genomes]
rs73671891	1.00[EUR][1000 genomes]
rs73672137	1.00[EUR][1000 genomes]
rs73672142	1.00[EUR][1000 genomes]
rs73672145	1.00[EUR][1000 genomes]
rs73672148	1.00[EUR][1000 genomes]
rs73672149	1.00[EUR][1000 genomes]
rs73672150	1.00[EUR][1000 genomes]
rs73672152	1.00[EUR][1000 genomes]
rs73672153	1.00[EUR][1000 genomes]
rs73673603	1.00[EUR][1000 genomes]
rs73673604	1.00[EUR][1000 genomes]
rs73673606	1.00[EUR][1000 genomes]
rs73673611	1.00[EUR][1000 genomes]
rs73673621	1.00[EUR][1000 genomes]
rs73673628	1.00[EUR][1000 genomes]
rs73673629	1.00[EUR][1000 genomes]
rs73673630	1.00[EUR][1000 genomes]
rs73673631	1.00[EUR][1000 genomes]
rs73673635	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673636	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673639	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673640	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673643	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673645	1.00[EUR][1000 genomes]
rs73673646	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673647	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673648	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673649	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73673650	1.00[EUR][1000 genomes]
rs73673654	1.00[EUR][1000 genomes]
rs73673655	1.00[EUR][1000 genomes]
rs73673657	1.00[EUR][1000 genomes]
rs73673659	1.00[EUR][1000 genomes]
rs73673662	1.00[EUR][1000 genomes]
rs73673665	1.00[EUR][1000 genomes]
rs73673666	1.00[EUR][1000 genomes]
rs73673667	1.00[EUR][1000 genomes]
rs73673671	1.00[EUR][1000 genomes]
rs73673672	1.00[EUR][1000 genomes]
rs73673683	1.00[EUR][1000 genomes]
rs73673687	1.00[EUR][1000 genomes]
rs7794298	1.00[EUR][1000 genomes]
rs7804113	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv916071	chr7:3423207-3697428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv887334	chr7:3531275-3635105	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1023888	chr7:3539750-3638242	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1034298	chr7:3539750-3646251	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv830888	chr7:3577214-3776276	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv1792280	chr7:3592290-3668229	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1017012	chr7:3602397-3638242	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv538679	chr7:3602397-3638242	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv605909	chr7:3605340-3638547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv948390	chr7:3609821-3734421	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv1033415	chr7:3616095-3753563	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv538680	chr7:3616095-3753563	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv1016930	chr7:3627295-3705057	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv530553	chr7:3629504-3736851	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3630400-3633400	Enhancers	H1 Cell Line	embryonic stem cell
2	chr7:3630600-3632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr7:3630800-3632800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr7:3630800-3633200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:3630800-3633400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:3630800-3633400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:3631000-3632800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:3631000-3632800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:3631000-3633200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:3631200-3636000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:3631600-3632800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:3631600-3633000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr7:3631800-3633000	Enhancers	HepG2	liver
14	chr7:3632000-3632800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:3632000-3632800	Active TSS	Brain Hippocampus Middle	brain
16	chr7:3632000-3632800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:3632000-3632800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr7:3632000-3633000	Enhancers	Fetal Lung	lung
19	chr7:3632200-3632800	Enhancers	Fetal Kidney	kidney
20	chr7:3632200-3632800	Active TSS	Stomach Mucosa	stomach
21	chr7:3632200-3632800	Active TSS	Osteobl	bone
22	chr7:3632200-3633000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:3632200-3633400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:3632200-3633400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:3632400-3632800	Enhancers	Brain Substantia Nigra	brain
26	chr7:3632400-3634600	Weak transcription	Fetal Brain Male	brain
27	chr7:3632600-3632800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr7:3632600-3632800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:3632600-3632800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr7:3632600-3633000	Enhancers	Primary B cells from cord blood	blood
31	chr7:3632600-3633200	Enhancers	Duodenum Mucosa	Duodenum
32	chr7:3632600-3633400	Enhancers	Pancreas	Pancrea
33	chr7:3632600-3638000	Weak transcription	Fetal Brain Female	brain

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