Variant report

Variant	rs7973067
Chromosome Location	chr12:123027814-123027815
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:123011807..123016958-chr12:123025504..123030876,9	K562	blood:
2	chr12:123027377..123029468-chr12:123032160..123034262,2	K562	blood:
3	chr12:123002522..123005008-chr12:123023951..123027966,3	K562	blood:

Variant related genes	Relation type
ENSG00000111011	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12301352	1.00[MEX][hapmap]
rs55817227	1.00[AMR][1000 genomes]
rs55935830	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs56019922	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56977093	0.92[AFR][1000 genomes]
rs56990369	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57142071	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57766838	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58276954	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58459934	0.92[AFR][1000 genomes]
rs60586933	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61062446	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61275910	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61585633	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6489161	1.00[AMR][1000 genomes]
rs7134209	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7297776	0.98[AFR][1000 genomes]
rs7307052	1.00[ASW][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7310898	1.00[ASW][hapmap];0.90[LWK][hapmap];0.88[MKK][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7960674	1.00[ASW][hapmap];0.85[LWK][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7961377	1.00[MEX][hapmap]
rs7972727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899570	chr12:122985057-123089209	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv1041677	chr12:122991478-123114125	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123012400-123029400	Weak transcription	Ovary	ovary
2	chr12:123012400-123035000	Weak transcription	Lung	lung
3	chr12:123012400-123036600	Weak transcription	Esophagus	oesophagus
4	chr12:123012400-123066000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:123012400-123114000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:123012400-123117000	Weak transcription	Pancreas	Pancrea
7	chr12:123012400-123121200	Weak transcription	Aorta	Aorta
8	chr12:123012600-123031600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr12:123012600-123032000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr12:123012600-123036600	Weak transcription	Left Ventricle	heart
11	chr12:123012600-123042600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:123012600-123066200	Weak transcription	Psoas Muscle	Psoas
13	chr12:123012600-123095600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:123012800-123032000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr12:123012800-123032000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr12:123012800-123036200	Weak transcription	Brain Anterior Caudate	brain
17	chr12:123012800-123036800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr12:123012800-123037200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr12:123012800-123037600	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr12:123012800-123042000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr12:123012800-123042000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr12:123012800-123065800	Weak transcription	Brain Substantia Nigra	brain
23	chr12:123012800-123097400	Weak transcription	Brain Angular Gyrus	brain
24	chr12:123012800-123109200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr12:123013000-123029400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr12:123013000-123029400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr12:123013000-123030800	Weak transcription	Adipose Nuclei	Adipose
28	chr12:123013000-123030800	Weak transcription	Fetal Lung	lung
29	chr12:123013000-123031800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr12:123013000-123037000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr12:123013000-123076400	Weak transcription	Right Ventricle	heart
32	chr12:123013000-123109200	Weak transcription	Colon Smooth Muscle	Colon
33	chr12:123013200-123034000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr12:123013200-123035200	Weak transcription	Liver	Liver
35	chr12:123013200-123036200	Weak transcription	Fetal Kidney	kidney
36	chr12:123013200-123036600	Weak transcription	Spleen	Spleen
37	chr12:123013200-123037600	Weak transcription	Small Intestine	intestine
38	chr12:123013200-123045800	Strong transcription	Fetal Thymus	thymus
39	chr12:123013200-123050000	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:123013200-123103000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:123013200-123112400	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr12:123013400-123041800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:123013400-123080600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:123013400-123107400	Weak transcription	Fetal Heart	heart
45	chr12:123013400-123120600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:123013600-123028400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
47	chr12:123013800-123050000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:123014400-123084000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr12:123014600-123085400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:123015400-123079800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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