Variant report

Variant	rs7760799
Chromosome Location	chr6:25499895-25499896
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:25498087..25500839-chr6:25503392..25507019,4	K562	blood:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10946784	0.86[EUR][1000 genomes]
rs12665641	0.86[EUR][1000 genomes]
rs16890653	0.91[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9356979	0.85[EUR][1000 genomes]
rs9358859	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9366625	0.85[EUR][1000 genomes]
rs9379770	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9379771	0.90[EUR][1000 genomes]
rs9393647	1.00[ASW][hapmap];0.91[CEU][hapmap];0.95[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9393648	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883487	chr6:25280119-25508868	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv830612	chr6:25342408-25509758	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25446800-25504400	Weak transcription	Primary B cells from cord blood	blood
2	chr6:25449400-25515800	Weak transcription	Lung	lung
3	chr6:25456400-25515800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:25456400-25537000	Weak transcription	Esophagus	oesophagus
5	chr6:25463200-25532200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:25464200-25518400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:25466400-25516000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:25466800-25515800	Weak transcription	Fetal Stomach	stomach
9	chr6:25471600-25597200	Weak transcription	Gastric	stomach
10	chr6:25473600-25516000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:25480000-25511400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:25480800-25523600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:25483000-25532200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:25484000-25500000	Weak transcription	HMEC	breast
15	chr6:25484600-25505800	Weak transcription	Aorta	Aorta
16	chr6:25484800-25515600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr6:25486400-25501600	Weak transcription	Fetal Brain Male	brain
18	chr6:25490400-25515800	Weak transcription	Thymus	Thymus
19	chr6:25490400-25521800	Weak transcription	GM12878-XiMat	blood
20	chr6:25490400-25543000	Weak transcription	Hela-S3	cervix
21	chr6:25490600-25524600	Weak transcription	A549	lung
22	chr6:25490800-25500000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:25490800-25500600	Weak transcription	Fetal Intestine Large	intestine
24	chr6:25490800-25506400	Weak transcription	Fetal Intestine Small	intestine
25	chr6:25490800-25511600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:25490800-25515800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr6:25490800-25515800	Weak transcription	Ovary	ovary
28	chr6:25490800-25516400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr6:25490800-25521400	Weak transcription	Small Intestine	intestine
30	chr6:25491600-25521000	Weak transcription	HSMMtube	muscle
31	chr6:25494000-25515400	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr6:25494000-25515600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:25494000-25551400	Weak transcription	Left Ventricle	heart
34	chr6:25494600-25515600	Weak transcription	Fetal Thymus	thymus
35	chr6:25495000-25515800	Weak transcription	Fetal Lung	lung
36	chr6:25495000-25516400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr6:25495400-25505000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr6:25495600-25501400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr6:25496000-25500000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr6:25496400-25500000	Weak transcription	NH-A	brain
41	chr6:25497400-25500400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:25497600-25500800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:25498000-25515800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:25498200-25500800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:25498400-25500800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:25498600-25502000	Strong transcription	Primary T cells from cord blood	blood
47	chr6:25498800-25500400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:25498800-25500600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:25498800-25500600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr6:25499000-25500600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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