Variant report

Variant	rs35956828
Chromosome Location	chr19:37073629-37073630
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:37062757..37066475-chr19:37067178..37075829,11	K562	blood:
2	chr19:37065150..37067798-chr19:37072514..37074047,2	K562	blood:

Variant related genes	Relation type
ENSG00000186020	Chromatin interaction
ENSG00000233527	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv833817	chr19:36978852-37195695	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
6	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	esv3334779	chr19:37050161-37076919	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	n/a
8	esv3434386	chr19:37073454-37114509	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv1323397	chr19:37073628-37073629	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37065600-37081200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:37065600-37095400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:37065800-37075200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:37065800-37076600	Weak transcription	Stomach Mucosa	stomach
5	chr19:37065800-37078200	Weak transcription	Right Ventricle	heart
6	chr19:37066000-37081200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr19:37066000-37081200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:37066600-37074200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr19:37066600-37074200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
10	chr19:37066600-37080600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr19:37066800-37074400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:37066800-37081000	Strong transcription	Dnd41	blood
13	chr19:37066800-37091400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:37067000-37073800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr19:37067000-37076200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr19:37067000-37076800	ZNF genes & repeats	GM12878-XiMat	blood
17	chr19:37067000-37080800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:37067000-37081200	ZNF genes & repeats	Liver	Liver
19	chr19:37067000-37081200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
20	chr19:37067400-37074600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
21	chr19:37067800-37074600	ZNF genes & repeats	Primary B cells from cord blood	blood
22	chr19:37068000-37074000	Strong transcription	Left Ventricle	heart
23	chr19:37068000-37074200	Strong transcription	Primary B cells from peripheral blood	blood
24	chr19:37068000-37074600	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr19:37068000-37074800	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr19:37068000-37074800	Strong transcription	Fetal Lung	lung
27	chr19:37068000-37075200	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr19:37068800-37076000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:37068800-37083000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr19:37070000-37095400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr19:37070200-37074000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
32	chr19:37070200-37074400	Strong transcription	HSMMtube	muscle
33	chr19:37070400-37074400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr19:37070600-37074400	ZNF genes & repeats	Ovary	ovary
35	chr19:37070600-37078400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr19:37070800-37076000	Weak transcription	Brain Anterior Caudate	brain
37	chr19:37071400-37079000	Weak transcription	NH-A	brain
38	chr19:37071800-37073800	Weak transcription	Colonic Mucosa	Colon
39	chr19:37072000-37073800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:37072000-37076000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
41	chr19:37072000-37081800	Weak transcription	HUVEC	blood vessel
42	chr19:37072200-37074000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:37072200-37075000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr19:37072200-37079400	Weak transcription	NHDF-Ad	bronchial
45	chr19:37072400-37074200	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr19:37072400-37074200	Weak transcription	Osteobl	bone
47	chr19:37072400-37074400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:37072400-37079200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:37072600-37074000	Weak transcription	Psoas Muscle	Psoas
50	chr19:37072600-37075000	Weak transcription	Fetal Kidney	kidney

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