Variant report

Variant	rs407710
Chromosome Location	chr6:33554257-33554258
allele	A/G
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:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33553164..33555974-chr6:33639876..33642136,2	MCF-7	breast:
2	chr6:33551460..33554975-chr6:33588078..33592105,4	K562	blood:
3	chr6:33553081..33555328-chr6:33667772..33669168,10	K562	blood:
4	chr6:33550022..33555745-chr6:33586647..33590467,5	MCF-7	breast:
5	chr6:33551901..33555908-chr6:33676752..33679381,5	K562	blood:
6	chr6:33240007..33241601-chr6:33553728..33555294,2	K562	blood:
7	chr6:33552057..33555351-chr6:33600748..33604007,3	MCF-7	breast:
8	chr6:33384196..33386645-chr6:33552574..33554724,2	MCF-7	breast:
9	chr6:33553773..33556336-chr6:33668184..33671160,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAK1-1	chr6:33553883-33555647	ENSG00000197251.3

No data

Variant related genes	Relation type
ENSG00000112514	Chromatin interaction
ENSG00000096433	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs210137	0.88[ASN][1000 genomes]
rs210138	0.88[ASN][1000 genomes]
rs210162	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs375555	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs530878	0.85[ASN][1000 genomes]
rs563751	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6900408	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462896	chr6:33534880-33588147	Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv602833	chr6:33534880-33588147	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885770	chr6:33543409-33614127	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv830638	chr6:33551202-33711346	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33548400-33557000	Weak transcription	HSMM	muscle
2	chr6:33548400-33557200	Weak transcription	NHDF-Ad	bronchial
3	chr6:33548400-33557600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:33548400-33557800	Weak transcription	Right Atrium	heart
5	chr6:33548600-33560600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:33548800-33557800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:33551800-33557200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:33552000-33557000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:33552600-33554600	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:33553000-33554400	Enhancers	Primary B cells from cord blood	blood
11	chr6:33553000-33554800	Enhancers	Spleen	Spleen
12	chr6:33553600-33554400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:33553600-33557000	Weak transcription	Ovary	ovary
14	chr6:33553600-33558000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr6:33553800-33554800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr6:33553800-33556400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:33553800-33556400	Weak transcription	Fetal Intestine Small	intestine
18	chr6:33553800-33556600	Weak transcription	Fetal Intestine Large	intestine
19	chr6:33553800-33556600	Weak transcription	Lung	lung
20	chr6:33553800-33556600	Weak transcription	Pancreas	Pancrea
21	chr6:33553800-33556800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr6:33553800-33556800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr6:33553800-33556800	Weak transcription	Stomach Mucosa	stomach
24	chr6:33553800-33557000	Weak transcription	Fetal Stomach	stomach
25	chr6:33553800-33557000	Weak transcription	HMEC	breast
26	chr6:33553800-33557000	Weak transcription	HSMMtube	muscle
27	chr6:33553800-33557200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:33553800-33557200	Weak transcription	Fetal Heart	heart
29	chr6:33553800-33557400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:33553800-33557400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:33553800-33557600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:33553800-33557600	Weak transcription	Left Ventricle	heart
33	chr6:33553800-33557600	Weak transcription	NH-A	brain
34	chr6:33553800-33557600	Weak transcription	Osteobl	bone
35	chr6:33553800-33557800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr6:33553800-33557800	Weak transcription	Esophagus	oesophagus
37	chr6:33553800-33558400	Weak transcription	Gastric	stomach
38	chr6:33553800-33560400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr6:33554000-33554400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr6:33554000-33554400	Enhancers	Stomach Smooth Muscle	stomach
41	chr6:33554000-33554400	Enhancers	Dnd41	blood
42	chr6:33554000-33554600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:33554000-33554600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:33554000-33555200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:33554000-33555400	Weak transcription	NHEK	skin
46	chr6:33554000-33555800	Weak transcription	Brain Anterior Caudate	brain
47	chr6:33554000-33556400	Weak transcription	Right Ventricle	heart
48	chr6:33554000-33556600	Weak transcription	Colonic Mucosa	Colon
49	chr6:33554000-33556600	Weak transcription	Hela-S3	cervix
50	chr6:33554000-33556600	Weak transcription	HUVEC	blood vessel

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