Variant report

Variant	rs35892030
Chromosome Location	chr12:64605728-64605729
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:64237164..64239543-chr12:64604173..64605904,2	MCF-7	breast:
2	chr12:64604646..64607427-chr12:64613216..64615906,2	K562	blood:
3	chr12:64561695..64564666-chr12:64604942..64606988,2	K562	blood:
4	chr12:64605413..64608740-chr12:64610311..64612005,3	K562	blood:
5	chr12:64600615..64607070-chr12:64614162..64618012,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000243024	Chromatin interaction
ENSG00000196935	Chromatin interaction
ENSG00000174206	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11831818	1.00[AMR][1000 genomes]
rs11834820	1.00[AMR][1000 genomes]
rs56015728	1.00[AMR][1000 genomes]
rs56684025	1.00[AMR][1000 genomes]
rs57378562	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58914823	1.00[AMR][1000 genomes]
rs59167764	1.00[AMR][1000 genomes]
rs73311817	1.00[AMR][1000 genomes]
rs73323059	1.00[AMR][1000 genomes]
rs73323067	1.00[AMR][1000 genomes]
rs74100222	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3351487	chr12:64420364-64763950	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv3509287	chr12:64526217-64736995	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	esv3509288	chr12:64526217-64736995	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64575000-64615200	Weak transcription	Psoas Muscle	Psoas
2	chr12:64575600-64607600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:64575600-64615000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr12:64575800-64615200	Weak transcription	Fetal Stomach	stomach
5	chr12:64576000-64615000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr12:64581400-64614600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr12:64581800-64615400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:64582600-64614600	Weak transcription	Hela-S3	cervix
9	chr12:64582600-64614600	Weak transcription	NHDF-Ad	bronchial
10	chr12:64583200-64615400	Weak transcription	Placenta	Placenta
11	chr12:64584800-64615200	Weak transcription	Thymus	Thymus
12	chr12:64586000-64611800	Weak transcription	Small Intestine	intestine
13	chr12:64586200-64615200	Weak transcription	Right Ventricle	heart
14	chr12:64587400-64609600	Weak transcription	K562	blood
15	chr12:64588200-64613000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr12:64588400-64605800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:64588400-64606200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:64588400-64606400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:64588400-64607200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:64588400-64613000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr12:64588400-64613000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr12:64588400-64614000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr12:64588400-64614600	Weak transcription	HMEC	breast
24	chr12:64588400-64614800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr12:64588400-64615000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr12:64588400-64615000	Weak transcription	HSMM	muscle
27	chr12:64588400-64615200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:64588400-64615400	Weak transcription	Spleen	Spleen
29	chr12:64588600-64606000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr12:64588600-64612400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr12:64589000-64607600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr12:64589000-64607600	Weak transcription	GM12878-XiMat	blood
33	chr12:64589000-64609600	Weak transcription	Gastric	stomach
34	chr12:64589000-64613000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr12:64589000-64613800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:64589000-64614800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr12:64589000-64614800	Weak transcription	Fetal Thymus	thymus
38	chr12:64589000-64615200	Weak transcription	Fetal Intestine Large	intestine
39	chr12:64589000-64615600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr12:64589200-64607800	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr12:64589200-64611800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:64589400-64612000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr12:64589400-64614600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:64589600-64612000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr12:64589800-64612400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:64594600-64615000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:64595200-64611800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:64595200-64613000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr12:64595600-64606000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:64595600-64609600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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