Variant report

Variant	rs2613899
Chromosome Location	chr12:74940148-74940149
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74939503..74941372-chr12:74990148..74991839,2	K562	blood:
2	chr12:74938864..74942058-chr12:74943211..74947418,4	K562	blood:
3	chr12:74934002..74935915-chr12:74937667..74942932,5	K562	blood:
4	chr12:74937896..74940364-chr12:74944289..74945994,2	K562	blood:
5	chr12:74933499..74938752-chr12:74938991..74943644,10	K562	blood:
6	chr12:74939663..74942006-chr12:74944132..74946349,2	MCF-7	breast:
7	chr12:74936725..74942637-chr12:74943509..74950364,10	MCF-7	breast:
8	chr12:74929872..74931969-chr12:74938974..74941515,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253719	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1037887	1.00[AFR][1000 genomes]
rs1389486	0.83[AFR][1000 genomes]
rs1389487	0.83[AFR][1000 genomes]
rs1389489	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1389490	1.00[AFR][1000 genomes]
rs1389491	1.00[AFR][1000 genomes]
rs1493798	1.00[AFR][1000 genomes]
rs1493804	1.00[AFR][1000 genomes]
rs1493807	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1563930	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1870699	1.00[AFR][1000 genomes]
rs1873987	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1873988	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2007674	1.00[AFR][1000 genomes]
rs2029717	1.00[AFR][1000 genomes]
rs2219608	1.00[AFR][1000 genomes]
rs2249335	0.83[AFR][1000 genomes]
rs2252250	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2605360	1.00[AFR][1000 genomes]
rs2605379	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2605380	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2613880	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2613892	1.00[AFR][1000 genomes]
rs2613896	1.00[AFR][1000 genomes]
rs2641465	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2925223	1.00[AFR][1000 genomes]
rs2925224	1.00[AFR][1000 genomes]
rs2926807	1.00[AFR][1000 genomes]
rs588875	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs590166	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs596999	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs625531	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs663854	1.00[AFR][1000 genomes]
rs694314	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs822806	1.00[YRI][hapmap]
rs822809	1.00[YRI][hapmap]
rs922222	0.83[AFR][1000 genomes]
rs970236	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899293	chr12:74835107-74995760	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv899295	chr12:74854750-74984992	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv470303	chr12:74880668-74945356	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	n/a
5	nsv899296	chr12:74880668-74974630	Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74933800-74942800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:74934200-74942000	Weak transcription	Ovary	ovary
3	chr12:74934600-74940800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr12:74935200-74940800	Weak transcription	Pancreas	Pancrea
5	chr12:74935200-74941000	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:74935200-74941800	Weak transcription	Thymus	Thymus
7	chr12:74935200-74942200	Weak transcription	Psoas Muscle	Psoas
8	chr12:74935200-74942600	Weak transcription	Small Intestine	intestine
9	chr12:74935200-74943600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:74935200-74945000	Weak transcription	Left Ventricle	heart
11	chr12:74935400-74942600	Weak transcription	Fetal Intestine Small	intestine
12	chr12:74935600-74941000	Weak transcription	Fetal Stomach	stomach
13	chr12:74935600-74941400	Weak transcription	Adipose Nuclei	Adipose
14	chr12:74935600-74942000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr12:74935600-74942400	Weak transcription	NHDF-Ad	bronchial
16	chr12:74935600-74943200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr12:74935800-74940400	Weak transcription	Hela-S3	cervix
18	chr12:74935800-74941000	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:74935800-74942800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:74936000-74942200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr12:74936000-74942400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:74936000-74942600	Weak transcription	Fetal Intestine Large	intestine
23	chr12:74936000-74945600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr12:74936200-74940200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr12:74936200-74940800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:74936200-74941200	Weak transcription	Fetal Thymus	thymus
27	chr12:74936200-74942600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:74936200-74943600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr12:74936400-74942000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:74936400-74945000	Weak transcription	Fetal Heart	heart
31	chr12:74936600-74941000	Weak transcription	Dnd41	blood
32	chr12:74936600-74942400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr12:74936800-74942000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:74936800-74942600	Weak transcription	Liver	Liver
35	chr12:74936800-74943000	Weak transcription	Primary T cells from cord blood	blood
36	chr12:74936800-74943200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:74937000-74940800	Weak transcription	Primary B cells from cord blood	blood
38	chr12:74937200-74942600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr12:74937600-74944400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:74937600-74944600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:74937800-74942800	Weak transcription	HSMM	muscle
42	chr12:74938200-74941400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:74938400-74941800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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