Variant report

Variant	rs74052507
Chromosome Location	chr1:10855778-10855779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
2	chr1:10838788..10840629-chr1:10854389..10855939,2	MCF-7	breast:
3	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
4	chr1:10854264..10855791-chr1:10891105..10892781,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs11121622	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv29966	chr1:10676800-10874152	Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv870849	chr1:10694125-10894724	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv529981	chr1:10697093-11353487	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
4	nsv832314	chr1:10704811-10859919	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	esv2757723	chr1:10742502-11055147	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	esv2758921	chr1:10742502-11055147	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv871772	chr1:10832322-10894724	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv870589	chr1:10840905-10901994	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv3353550	chr1:10853540-10857138	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv3438070	chr1:10855190-10857938	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10853000-10857200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr1:10853200-10856200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
3	chr1:10853200-10856200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
4	chr1:10853200-10857000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr1:10853200-10857000	Active TSS	Duodenum Mucosa	Duodenum
6	chr1:10853200-10857000	Active TSS	Psoas Muscle	Psoas
7	chr1:10853200-10857200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr1:10853200-10857200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:10853400-10856000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
10	chr1:10853400-10856000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:10853400-10856400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
12	chr1:10853400-10856600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:10853400-10856800	Active TSS	Esophagus	oesophagus
14	chr1:10853400-10856800	Active TSS	Left Ventricle	heart
15	chr1:10853400-10856800	Active TSS	Right Atrium	heart
16	chr1:10853400-10857000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
17	chr1:10853400-10857200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
18	chr1:10853600-10856800	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr1:10853600-10856800	Active TSS	Aorta	Aorta
20	chr1:10853600-10856800	Active TSS	HSMMtube	muscle
21	chr1:10853600-10857000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:10853600-10857000	Active TSS	Rectal Mucosa Donor 31	rectum
23	chr1:10853600-10857000	Bivalent/Poised TSS	Thymus	Thymus
24	chr1:10853600-10857200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr1:10853600-10857200	Bivalent Enhancer	Fetal Brain Male	brain
26	chr1:10853800-10855800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
27	chr1:10853800-10856000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
28	chr1:10853800-10856000	Flanking Active TSS	Liver	Liver
29	chr1:10853800-10856400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:10853800-10856600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr1:10853800-10856800	Active TSS	Lung	lung
32	chr1:10853800-10857000	Enhancers	Primary B cells from cord blood	blood
33	chr1:10853800-10857000	Active TSS	Gastric	stomach
34	chr1:10853800-10857200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr1:10854000-10855800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
36	chr1:10854000-10856000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:10854200-10856000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:10854200-10856200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:10854400-10857000	Active TSS	Rectal Smooth Muscle	rectum
40	chr1:10854600-10856000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr1:10854600-10856600	Active TSS	Stomach Mucosa	stomach
42	chr1:10854600-10857000	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr1:10854600-10857200	Active TSS	Right Ventricle	heart
44	chr1:10854800-10856000	Bivalent Enhancer	Fetal Thymus	thymus
45	chr1:10854800-10856200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:10854800-10856200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr1:10854800-10856400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
48	chr1:10854800-10856400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:10854800-10856800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:10854800-10856800	Active TSS	Pancreas	Pancrea

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