Variant report

Variant	rs1871628
Chromosome Location	chr10:1160736-1160737
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:1155917..1158067-chr10:1158986..1161390,4	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1079387	0.85[YRI][hapmap]
rs10794716	1.00[MEX][hapmap]
rs11250238	0.85[YRI][hapmap]
rs11250259	1.00[AMR][1000 genomes]
rs1135416	0.92[YRI][hapmap]
rs1871627	1.00[AMR][1000 genomes]
rs2086381	1.00[AMR][1000 genomes]
rs4403737	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs4880762	1.00[AMR][1000 genomes]
rs4880764	1.00[ASW][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[AMR][1000 genomes]
rs7068520	1.00[AMR][1000 genomes]
rs7071817	0.91[YRI][hapmap];1.00[AMR][1000 genomes]
rs7091153	1.00[AMR][1000 genomes]
rs9783192	1.00[AMR][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	chr10:1144800-1232600	Weak transcription	Right Atrium	heart
15	chr10:1146800-1167800	Weak transcription	Fetal Heart	heart
16	chr10:1149200-1173200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr10:1149600-1173600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr10:1153000-1165600	Strong transcription	Primary hematopoietic stem cells	blood
19	chr10:1153200-1175000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr10:1154000-1161000	Weak transcription	Small Intestine	intestine
21	chr10:1154000-1161600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr10:1154000-1164600	Weak transcription	Fetal Brain Male	brain
23	chr10:1154000-1177200	Weak transcription	Stomach Mucosa	stomach
24	chr10:1154600-1162000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr10:1155000-1163200	Weak transcription	Hela-S3	cervix
26	chr10:1155400-1163400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:1156200-1168600	Strong transcription	Aorta	Aorta
28	chr10:1156400-1177400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr10:1156600-1163200	Weak transcription	A549	lung
30	chr10:1156600-1165600	Strong transcription	Fetal Intestine Large	intestine
31	chr10:1156600-1169200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr10:1156600-1169200	Strong transcription	GM12878-XiMat	blood
33	chr10:1156600-1171800	Strong transcription	Osteobl	bone
34	chr10:1156600-1179000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:1156800-1160800	Strong transcription	Left Ventricle	heart
36	chr10:1156800-1162800	Strong transcription	Fetal Thymus	thymus
37	chr10:1156800-1164600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr10:1156800-1165600	Strong transcription	Duodenum Mucosa	Duodenum
39	chr10:1156800-1165800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr10:1156800-1166200	Strong transcription	Fetal Intestine Small	intestine
41	chr10:1156800-1166200	Strong transcription	Fetal Muscle Trunk	muscle
42	chr10:1156800-1168400	Strong transcription	Dnd41	blood
43	chr10:1156800-1170000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:1156800-1177800	Strong transcription	Spleen	Spleen
45	chr10:1156800-1178800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:1156800-1179400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr10:1157000-1160800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:1157000-1160800	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr10:1157000-1162800	Strong transcription	Primary T cells from cord blood	blood
50	chr10:1157000-1162800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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