Variant report

Variant	rs11250267
Chromosome Location	chr10:1156487-1156488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:1154681..1157651-chr10:1165261..1167204,2	MCF-7	breast:
2	chr10:1156155..1156681-chr10:1410890..1411623,2	K562	blood:
3	chr10:1150337..1153151-chr10:1154586..1158431,3	K562	blood:
4	chr10:1156343..1159152-chr10:1169423..1170995,2	K562	blood:
5	chr10:1155977..1157935-chr10:1333805..1335965,2	MCF-7	breast:
6	chr10:1155649..1156639-chr10:1410710..1411699,3	MCF-7	breast:
7	chr10:1155917..1158067-chr10:1158986..1161390,4	MCF-7	breast:
8	chr10:1155889..1157522-chr10:1215950..1218496,2	K562	blood:

Variant related genes	Relation type
ENSG00000047056	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2101051	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34034003	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs36051896	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7091502	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72760941	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72760943	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1050577	chr10:986723-1277854	Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv540409	chr10:986723-1277854	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv949405	chr10:1010464-1376105	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv894722	chr10:1058837-1274538	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	nsv1046220	chr10:1064024-1188998	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
14	nsv894723	chr10:1073684-1259485	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
15	nsv894725	chr10:1110464-1421516	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
16	nsv1054432	chr10:1115626-1230431	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv1041498	chr10:1117200-1760190	Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
18	nsv894726	chr10:1151620-1216861	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1117800-1168600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr10:1118000-1168400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:1118000-1173800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:1122200-1168400	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr10:1122600-1168800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr10:1123000-1168600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:1123200-1178400	Strong transcription	Liver	Liver
8	chr10:1123400-1177800	Strong transcription	Primary B cells from peripheral blood	blood
9	chr10:1124200-1178000	Strong transcription	Primary B cells from cord blood	blood
10	chr10:1127800-1179000	Strong transcription	Fetal Stomach	stomach
11	chr10:1129400-1179000	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr10:1138600-1162800	Strong transcription	Thymus	Thymus
13	chr10:1138600-1178600	Strong transcription	Adipose Nuclei	Adipose
14	chr10:1138800-1159400	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr10:1139200-1157200	Strong transcription	Fetal Brain Female	brain
16	chr10:1139600-1160000	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr10:1144800-1232600	Weak transcription	Right Atrium	heart
18	chr10:1146600-1158200	Strong transcription	Rectal Smooth Muscle	rectum
19	chr10:1146800-1158200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:1146800-1167800	Weak transcription	Fetal Heart	heart
21	chr10:1149000-1157600	Strong transcription	Skeletal Muscle Male	skeletal muscle
22	chr10:1149200-1159800	Strong transcription	HSMMtube	muscle
23	chr10:1149200-1173200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:1149600-1173600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr10:1152600-1157000	Strong transcription	Brain Substantia Nigra	brain
26	chr10:1153000-1165600	Strong transcription	Primary hematopoietic stem cells	blood
27	chr10:1153200-1175000	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr10:1153400-1157000	Strong transcription	Fetal Muscle Leg	muscle
29	chr10:1153800-1156600	Strong transcription	Pancreas	Pancrea
30	chr10:1154000-1158200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr10:1154000-1158400	Weak transcription	Brain Angular Gyrus	brain
32	chr10:1154000-1161000	Weak transcription	Small Intestine	intestine
33	chr10:1154000-1161600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr10:1154000-1164600	Weak transcription	Fetal Brain Male	brain
35	chr10:1154000-1177200	Weak transcription	Stomach Mucosa	stomach
36	chr10:1154400-1157000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr10:1154600-1158200	Weak transcription	Fetal Kidney	kidney
38	chr10:1154600-1162000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr10:1155000-1158400	Weak transcription	Psoas Muscle	Psoas
40	chr10:1155000-1160200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr10:1155000-1160400	Weak transcription	Colon Smooth Muscle	Colon
42	chr10:1155000-1163200	Weak transcription	Hela-S3	cervix
43	chr10:1155200-1157400	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr10:1155200-1157400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr10:1155200-1157600	Weak transcription	Brain Hippocampus Middle	brain
46	chr10:1155200-1158000	Weak transcription	Ovary	ovary
47	chr10:1155200-1158200	Weak transcription	Fetal Lung	lung
48	chr10:1155400-1158000	Weak transcription	Brain Anterior Caudate	brain
49	chr10:1155400-1163400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:1155600-1156600	Genic enhancers	HepG2	liver

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