Variant report

Variant	rs61777360
Chromosome Location	chr1:10853981-10853982
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:10712004..10714801-chr1:10852157..10855382,3	MCF-7	breast:
2	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
3	chr1:10852601..10855720-chr1:10959417..10961902,3	MCF-7	breast:
4	chr1:10841137..10843114-chr1:10851742..10854578,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs28716527	1.00[AMR][1000 genomes]
rs61775159	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6673483	1.00[AMR][1000 genomes]
rs6681793	1.00[AMR][1000 genomes]
rs74052531	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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

No data

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10853000-10857200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr1:10853200-10854000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
3	chr1:10853200-10854000	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr1:10853200-10854200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
5	chr1:10853200-10854200	Active TSS	Right Ventricle	heart
6	chr1:10853200-10854200	Active TSS	Stomach Smooth Muscle	stomach
7	chr1:10853200-10854400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
8	chr1:10853200-10854400	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr1:10853200-10856200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
10	chr1:10853200-10856200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
11	chr1:10853200-10857000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr1:10853200-10857000	Active TSS	Duodenum Mucosa	Duodenum
13	chr1:10853200-10857000	Active TSS	Psoas Muscle	Psoas
14	chr1:10853200-10857200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
15	chr1:10853200-10857200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:10853400-10854000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:10853400-10854000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
18	chr1:10853400-10854000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
19	chr1:10853400-10854000	Active TSS	Colonic Mucosa	Colon
20	chr1:10853400-10854000	Bivalent/Poised TSS	Ovary	ovary
21	chr1:10853400-10854000	Bivalent Enhancer	HUVEC	blood vessel
22	chr1:10853400-10854200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:10853400-10854200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
24	chr1:10853400-10854200	Bivalent Enhancer	Placenta	Placenta
25	chr1:10853400-10854400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr1:10853400-10854400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
27	chr1:10853400-10854400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:10853400-10854400	Active TSS	Fetal Intestine Large	intestine
29	chr1:10853400-10854400	Active TSS	Pancreas	Pancrea
30	chr1:10853400-10854600	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr1:10853400-10854800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:10853400-10854800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
33	chr1:10853400-10855200	Active TSS	Colon Smooth Muscle	Colon
34	chr1:10853400-10855600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr1:10853400-10856000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
36	chr1:10853400-10856000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:10853400-10856400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
38	chr1:10853400-10856600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:10853400-10856800	Active TSS	Esophagus	oesophagus
40	chr1:10853400-10856800	Active TSS	Left Ventricle	heart
41	chr1:10853400-10856800	Active TSS	Right Atrium	heart
42	chr1:10853400-10857000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
43	chr1:10853400-10857200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:10853600-10854000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:10853600-10854000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:10853600-10854000	Active TSS	HMEC	breast
47	chr1:10853600-10854200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
48	chr1:10853600-10854200	Bivalent/Poised TSS	Fetal Lung	lung
49	chr1:10853600-10854200	Bivalent/Poised TSS	Fetal Stomach	stomach
50	chr1:10853600-10854200	Active TSS	Skeletal Muscle Male	skeletal muscle

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