Variant report

Variant	rs189131378
Chromosome Location	chr6:128421000-128421001
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 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	nsv604643	chr6:128359362-128493991	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv604644	chr6:128394889-128486139	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	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
6	nsv516794	chr6:128403745-128430506	Flanking Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv886650	chr6:128403745-128513395	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1031827	chr6:128418702-128497881	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2763955	chr6:128418714-128436415	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv5471	chr6:128419437-128430379	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128289000-128431000	Weak transcription	Psoas Muscle	Psoas
2	chr6:128375000-128433800	Weak transcription	Aorta	Aorta
3	chr6:128379000-128432800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:128399000-128422600	Weak transcription	HUVEC	blood vessel
5	chr6:128401400-128431800	Weak transcription	Right Ventricle	heart
6	chr6:128401800-128433600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:128403800-128421600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:128404000-128438000	Weak transcription	Fetal Thymus	thymus
9	chr6:128404400-128422000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:128405000-128431400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:128406600-128433000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr6:128410400-128421200	Weak transcription	NHEK	skin
13	chr6:128411000-128433600	Weak transcription	HSMMtube	muscle
14	chr6:128411200-128424600	Weak transcription	Fetal Intestine Small	intestine
15	chr6:128411200-128433800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:128411200-128433800	Weak transcription	Fetal Stomach	stomach
17	chr6:128411200-128433800	Weak transcription	Ovary	ovary
18	chr6:128411600-128445600	Weak transcription	HepG2	liver
19	chr6:128418400-128422400	Weak transcription	Liver	Liver
20	chr6:128419600-128421000	Weak transcription	Brain Anterior Caudate	brain
21	chr6:128419600-128421000	Enhancers	Brain Hippocampus Middle	brain
22	chr6:128419800-128424000	Weak transcription	Pancreas	Pancrea
23	chr6:128419800-128424200	Weak transcription	Left Ventricle	heart
24	chr6:128419800-128424200	Weak transcription	Right Atrium	heart
25	chr6:128419800-128424600	Weak transcription	Gastric	stomach
26	chr6:128419800-128434800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:128419800-128455600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:128420000-128421000	Weak transcription	Fetal Heart	heart
29	chr6:128420400-128421400	Enhancers	Brain Substantia Nigra	brain
30	chr6:128420600-128421400	Enhancers	Brain Cingulate Gyrus	brain
31	chr6:128420800-128421000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:128420800-128421000	Enhancers	Brain Angular Gyrus	brain
33	chr6:128420800-128421000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr6:128420800-128421200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr6:128420800-128421400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:128420800-128421400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:128420800-128421400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:128420800-128421400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:128421000-128421200	Enhancers	Brain Anterior Caudate	brain
40	chr6:128421000-128421200	Enhancers	Fetal Heart	heart
41	chr6:128421000-128421400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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