Variant report

Variant	rs12097637
Chromosome Location	chr1:62388995-62388996
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr1:62388795-62389044	SH-SY5Y	brain:	n/a	n/a

Variant related genes	Relation type
INADL	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10047078	0.83[AMR][1000 genomes]
rs10889274	0.83[AMR][1000 genomes]
rs10889275	0.83[AMR][1000 genomes]
rs10889276	0.83[AMR][1000 genomes]
rs11207867	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207871	0.83[AMR][1000 genomes]
rs11207873	0.83[YRI][hapmap];0.83[AMR][1000 genomes]
rs11207875	0.83[AMR][1000 genomes]
rs11485616	0.83[AMR][1000 genomes]
rs11801545	0.83[AMR][1000 genomes]
rs11802946	0.83[AMR][1000 genomes]
rs11804624	0.83[AMR][1000 genomes]
rs11807297	0.83[LWK][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs11809363	0.83[LWK][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs11811508	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12064034	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12064276	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12069154	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12069359	0.83[AMR][1000 genomes]
rs12070855	0.87[LWK][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs12074521	0.83[AMR][1000 genomes]
rs12085283	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12086149	0.84[YRI][hapmap]
rs12097605	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12239276	0.83[AMR][1000 genomes]
rs41365548	0.87[LWK][hapmap];1.00[MEX][hapmap]
rs61743112	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74076821	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74076835	0.83[AMR][1000 genomes]
rs9970060	0.83[AMR][1000 genomes]
rs9970292	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693319	chr1:62207254-62402549	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv518627	chr1:62279594-62517947	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv522020	chr1:62279594-62517947	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv531876	chr1:62302313-62504349	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62317800-62390400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr1:62336000-62408600	Weak transcription	Pancreas	Pancrea
3	chr1:62340400-62399200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:62346000-62389400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:62346200-62417600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr1:62350200-62397600	Weak transcription	Esophagus	oesophagus
7	chr1:62350600-62391600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr1:62350800-62395800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:62350800-62397800	Weak transcription	Primary T cells from cord blood	blood
11	chr1:62350800-62417600	Weak transcription	Ovary	ovary
12	chr1:62353600-62396000	Weak transcription	Fetal Kidney	kidney
13	chr1:62353800-62408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:62361200-62390800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:62361600-62391800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:62361600-62408800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:62362000-62408600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:62363000-62391800	Weak transcription	Stomach Mucosa	stomach
19	chr1:62363400-62391400	Weak transcription	A549	lung
20	chr1:62372400-62408800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:62372400-62417600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:62374600-62410600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr1:62375200-62404600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr1:62376200-62417600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:62377200-62396600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:62379400-62393600	Weak transcription	Right Ventricle	heart
27	chr1:62379800-62392800	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr1:62380600-62408600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr1:62380800-62390200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:62380800-62395800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr1:62380800-62410000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:62381000-62393200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:62381000-62393600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr1:62381000-62408200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr1:62381000-62416000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr1:62381200-62394600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:62381200-62417400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr1:62381200-62418400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:62381600-62402800	Weak transcription	HepG2	liver
40	chr1:62382400-62393400	Weak transcription	Liver	Liver
41	chr1:62383400-62408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:62384600-62391800	Weak transcription	Gastric	stomach
43	chr1:62384600-62403000	Weak transcription	Fetal Stomach	stomach
44	chr1:62384600-62408200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:62384600-62408800	Weak transcription	Fetal Intestine Large	intestine
46	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
47	chr1:62385400-62394800	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr1:62385400-62408400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:62385400-62408600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr1:62386000-62394800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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