Variant report

Variant	rs535446143
Chromosome Location	chr6:33725933-33725934
allele	C/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	chr6:33724784..33727400-chr6:33728214..33730024,2	MCF-7	breast:
2	chr6:33697291..33699933-chr6:33725185..33727883,2	MCF-7	breast:
3	chr6:33724946..33727778-chr6:33732399..33734777,2	MCF-7	breast:
4	chr6:33725418..33728218-chr6:33736581..33739360,2	MCF-7	breast:
5	chr6:33712420..33715409-chr6:33723991..33728116,4	MCF-7	breast:
6	chr6:33723585..33725981-chr6:33736190..33738429,2	MCF-7	breast:
7	chr6:33711077..33714000-chr6:33723904..33727038,3	MCF-7	breast:
8	chr6:33725421..33728114-chr6:33818801..33821160,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000161896	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885772	chr6:33638180-33767727	Bivalent Enhancer Genic enhancers Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv462897	chr6:33717770-33778964	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv602839	chr6:33717770-33778964	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription 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	11 gene(s)	inside rSNPs	diseases
4	nsv462898	chr6:33723383-33768897	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv602840	chr6:33723383-33768897	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	esv3475116	chr6:33725038-33726834	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3475117	chr6:33725169-33726743	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33715200-33737800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:33715600-33729400	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr6:33719600-33729000	Weak transcription	Right Atrium	heart
4	chr6:33719800-33727600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:33719800-33729200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:33720200-33728000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:33720200-33730600	Weak transcription	Spleen	Spleen
8	chr6:33720400-33728000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:33720600-33729400	Weak transcription	Fetal Intestine Large	intestine
10	chr6:33720800-33726200	Weak transcription	Fetal Lung	lung
11	chr6:33721000-33727000	Weak transcription	Fetal Intestine Small	intestine
12	chr6:33721000-33729400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:33721200-33728600	Weak transcription	Fetal Thymus	thymus
14	chr6:33723400-33729800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:33723400-33736600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr6:33723600-33727800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr6:33723600-33728200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:33723600-33728800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:33723600-33729000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:33724000-33730200	Enhancers	Stomach Mucosa	stomach
21	chr6:33725000-33726400	Enhancers	Placenta	Placenta
22	chr6:33725000-33728800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:33725200-33726200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:33725200-33729200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr6:33725200-33729600	Weak transcription	Stomach Smooth Muscle	stomach
26	chr6:33725200-33729800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr6:33725400-33726000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr6:33725400-33726800	Enhancers	Hela-S3	cervix
29	chr6:33725600-33726400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:33725800-33726000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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