Variant report

Variant	rs7771935
Chromosome Location	chr6:34350429-34350430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34339964..34342823-chr6:34350298..34352076,2	K562	blood:
2	chr6:34203417..34205064-chr6:34349591..34351269,2	K562	blood:
3	chr6:34350156..34353339-chr6:34359370..34361777,7	MCF-7	breast:
4	chr6:34342887..34344725-chr6:34348668..34351040,2	K562	blood:
5	chr6:34215496..34218405-chr6:34348666..34350729,2	K562	blood:
6	chr6:34349500..34351699-chr6:34352826..34355839,3	K562	blood:

Variant related genes	Relation type
ENSG00000137309	Chromatin interaction
ENSG00000186577	Chromatin interaction
ENSG00000272325	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs58600226	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60933648	1.00[AMR][1000 genomes]
rs6912357	1.00[AMR][1000 genomes]
rs6931339	1.00[AMR][1000 genomes]
rs7739644	1.00[AMR][1000 genomes]
rs7740217	1.00[AMR][1000 genomes]
rs7750807	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7764155	1.00[AMR][1000 genomes]
rs7764521	1.00[AMR][1000 genomes]
rs7769855	1.00[AMR][1000 genomes]
rs7773228	1.00[AMR][1000 genomes]
rs7775790	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv1034978	chr6:34327526-34362187	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34315400-34351200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:34318200-34355800	Weak transcription	Brain Germinal Matrix	brain
3	chr6:34327000-34351600	Weak transcription	Ovary	ovary
4	chr6:34327800-34356400	Weak transcription	Hela-S3	cervix
5	chr6:34328000-34351200	Weak transcription	Gastric	stomach
6	chr6:34328600-34358000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:34329800-34351200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:34331000-34358400	Weak transcription	Aorta	Aorta
9	chr6:34331200-34351600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr6:34331400-34351400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:34331400-34353400	Weak transcription	Small Intestine	intestine
12	chr6:34331400-34353600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:34331600-34351400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:34331600-34353600	Weak transcription	Fetal Intestine Large	intestine
15	chr6:34333600-34358000	Weak transcription	HMEC	breast
16	chr6:34335200-34354600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:34335600-34358800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:34337800-34359000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr6:34338000-34353600	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:34338200-34351600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:34338200-34358600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr6:34338400-34351000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr6:34338400-34353600	Weak transcription	Pancreas	Pancrea
24	chr6:34338400-34356600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr6:34338600-34351200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:34338600-34351800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:34338800-34351400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:34339200-34351200	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:34339200-34358000	Weak transcription	NHEK	skin
30	chr6:34339400-34358000	Weak transcription	HUVEC	blood vessel
31	chr6:34340400-34358000	Weak transcription	Fetal Thymus	thymus
32	chr6:34341000-34351800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr6:34341600-34351200	Weak transcription	Right Atrium	heart
34	chr6:34342600-34351000	Weak transcription	Brain Angular Gyrus	brain
35	chr6:34342600-34351000	Weak transcription	Brain Anterior Caudate	brain
36	chr6:34342600-34351000	Weak transcription	Brain Hippocampus Middle	brain
37	chr6:34342600-34351000	Weak transcription	Colon Smooth Muscle	Colon
38	chr6:34342600-34351200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr6:34342600-34351200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr6:34342600-34351200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr6:34342600-34355800	Weak transcription	Fetal Brain Female	brain
42	chr6:34342800-34353800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:34343000-34351200	Weak transcription	GM12878-XiMat	blood
44	chr6:34343000-34357600	Weak transcription	Primary hematopoietic stem cells	blood
45	chr6:34343400-34356600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr6:34344000-34353800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:34344800-34351600	Weak transcription	Psoas Muscle	Psoas
48	chr6:34345000-34351200	Weak transcription	Fetal Heart	heart
49	chr6:34345200-34351000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr6:34345200-34358600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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