Variant report

Variant	rs371956972
Chromosome Location	chr6:128767089-128767090
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886649	chr6:128399657-128808054	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv830800	chr6:128710631-128878435	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv3354843	chr6:128765959-128767257	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128740800-128777000	Weak transcription	Fetal Intestine Small	intestine
2	chr6:128753200-128777000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:128756400-128776600	Weak transcription	Fetal Intestine Large	intestine
4	chr6:128759800-128767200	Weak transcription	HMEC	breast
5	chr6:128759800-128767400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:128759800-128786800	Weak transcription	Left Ventricle	heart
7	chr6:128760200-128769800	Weak transcription	Brain Angular Gyrus	brain
8	chr6:128760800-128767400	Weak transcription	Brain Anterior Caudate	brain
9	chr6:128761400-128775600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:128761400-128778000	Weak transcription	Small Intestine	intestine
11	chr6:128762800-128767200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:128762800-128774800	Weak transcription	Ovary	ovary
13	chr6:128763000-128771800	Weak transcription	Fetal Kidney	kidney
14	chr6:128763200-128773200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:128763600-128775200	Weak transcription	Psoas Muscle	Psoas
16	chr6:128765400-128769200	Weak transcription	Gastric	stomach
17	chr6:128765600-128767400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:128765600-128775200	Weak transcription	Pancreas	Pancrea
19	chr6:128765800-128777000	Weak transcription	HepG2	liver
20	chr6:128766000-128767200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:128766800-128767600	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr6:128766800-128768000	Enhancers	Fetal Brain Male	brain
23	chr6:128766800-128768200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:128767000-128767200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:128767000-128767400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr6:128767000-128767800	Enhancers	Fetal Brain Female	brain
27	chr6:128767000-128767800	Enhancers	NHEK	skin
28	chr6:128767000-128768000	Enhancers	HUES48 Cell Line	embryonic stem cell

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