Variant report

Variant	rs10845575
Chromosome Location	chr12:12707576-12707577
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:12706288..12708434-chr12:12738736..12740551,2	MCF-7	breast:
2	chr12:12705696..12707891-chr12:12708023..12709749,2	K562	blood:
3	chr12:12672115..12676410-chr12:12705674..12709686,5	K562	blood:

Variant related genes	Relation type
ENSG00000111266	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10845576	0.82[ASN][1000 genomes]
rs4579996	0.87[ASN][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	esv2758295	chr12:12620654-12783124	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv2759880	chr12:12620654-12783124	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv898811	chr12:12655443-12928295	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12686600-12708000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:12686600-12711400	Weak transcription	Esophagus	oesophagus
3	chr12:12686800-12712200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:12686800-12712600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:12687200-12708000	Weak transcription	Right Ventricle	heart
6	chr12:12687200-12711600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:12687200-12712600	Weak transcription	Aorta	Aorta
8	chr12:12687400-12708000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr12:12687400-12708000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:12687400-12710600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr12:12687400-12712600	Weak transcription	K562	blood
12	chr12:12688200-12710800	Weak transcription	Pancreas	Pancrea
13	chr12:12688200-12714400	Weak transcription	Gastric	stomach
14	chr12:12689600-12708000	Weak transcription	Ovary	ovary
15	chr12:12690600-12712600	Weak transcription	NHLF	lung
16	chr12:12690800-12710400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr12:12692000-12713000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:12692400-12713600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:12692600-12708000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:12692600-12708000	Weak transcription	Small Intestine	intestine
21	chr12:12694200-12708000	Weak transcription	Left Ventricle	heart
22	chr12:12694200-12712800	Weak transcription	Adipose Nuclei	Adipose
23	chr12:12694400-12708000	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr12:12694400-12712800	Weak transcription	Fetal Muscle Trunk	muscle
25	chr12:12694400-12712800	Weak transcription	Fetal Stomach	stomach
26	chr12:12694600-12710800	Weak transcription	Fetal Muscle Leg	muscle
27	chr12:12694600-12711600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:12694600-12711600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr12:12694600-12712600	Weak transcription	Fetal Thymus	thymus
30	chr12:12694800-12710800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr12:12696200-12710400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:12697600-12712600	Weak transcription	Thymus	Thymus
33	chr12:12698800-12712400	Weak transcription	NHEK	skin
34	chr12:12699000-12712600	Weak transcription	HUVEC	blood vessel
35	chr12:12699600-12712600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:12699800-12708000	Weak transcription	Brain Angular Gyrus	brain
37	chr12:12699800-12708000	Weak transcription	Fetal Intestine Large	intestine
38	chr12:12699800-12709800	Weak transcription	Fetal Kidney	kidney
39	chr12:12700000-12707800	Weak transcription	Fetal Heart	heart
40	chr12:12700000-12712000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr12:12700400-12712600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr12:12700800-12707800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr12:12701000-12711000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr12:12701000-12711400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr12:12701200-12711600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:12701400-12708000	Weak transcription	Right Atrium	heart
47	chr12:12701400-12708200	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr12:12701400-12709200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr12:12701400-12710800	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr12:12701400-12712600	Weak transcription	Fetal Lung	lung

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