Variant report

Variant	rs377215508
Chromosome Location	chr3:142150717-142150718
allele	-/TA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:142145919..142149296-chr3:142150484..142152821,3	K562	blood:

Variant related genes	Relation type
ENSG00000114127	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv522549	chr3:141812759-142164735	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv877556	chr3:141898980-142331360	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS 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	51 gene(s)	inside rSNPs	diseases
4	nsv523945	chr3:141933649-142219542	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv1000083	chr3:141956718-142172666	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv877558	chr3:142123841-142331360	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	nsv523596	chr3:142132749-142164735	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv877559	chr3:142132749-142331360	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	esv3427207	chr3:142149962-142152010	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	esv1079383	chr3:142150692-142150720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142083600-142158600	Weak transcription	NHEK	skin
2	chr3:142105000-142151800	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr3:142106800-142150800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:142112200-142151600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr3:142112200-142152000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr3:142112200-142152200	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr3:142112200-142154600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr3:142113000-142152200	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:142113400-142151800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:142114800-142151800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:142120400-142151800	Strong transcription	Primary B cells from peripheral blood	blood
13	chr3:142120600-142151800	Strong transcription	Dnd41	blood
14	chr3:142125000-142151800	Strong transcription	Fetal Thymus	thymus
15	chr3:142127000-142152000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:142127200-142152200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:142127400-142159600	Weak transcription	Psoas Muscle	Psoas
18	chr3:142131600-142156000	Weak transcription	Fetal Heart	heart
19	chr3:142134200-142152600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr3:142136400-142157400	Weak transcription	HMEC	breast
21	chr3:142136800-142150800	Strong transcription	Liver	Liver
22	chr3:142138600-142158600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:142138600-142164600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:142138800-142163000	Weak transcription	Spleen	Spleen
25	chr3:142139200-142151200	Weak transcription	Right Ventricle	heart
26	chr3:142139400-142156200	Weak transcription	Small Intestine	intestine
27	chr3:142139400-142157000	Weak transcription	Brain Germinal Matrix	brain
28	chr3:142139400-142158600	Weak transcription	Pancreas	Pancrea
29	chr3:142139400-142163200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:142141200-142157000	Weak transcription	Esophagus	oesophagus
31	chr3:142141600-142162400	Weak transcription	Brain Angular Gyrus	brain
32	chr3:142142200-142151200	Weak transcription	Hela-S3	cervix
33	chr3:142142200-142165400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:142142400-142153400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:142142800-142153200	Weak transcription	HUVEC	blood vessel
36	chr3:142143600-142151800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:142144200-142151600	Strong transcription	Adipose Nuclei	Adipose
38	chr3:142145800-142151400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr3:142145800-142152200	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr3:142146000-142151800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:142146200-142151800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:142146400-142151600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr3:142146400-142151800	Strong transcription	Fetal Intestine Large	intestine
44	chr3:142146600-142151600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr3:142146600-142151600	Strong transcription	Fetal Muscle Leg	muscle
46	chr3:142146600-142151600	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr3:142146600-142152200	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr3:142146600-142152200	Strong transcription	Stomach Smooth Muscle	stomach
49	chr3:142146600-142164200	Weak transcription	Stomach Mucosa	stomach
50	chr3:142147000-142151800	Strong transcription	Primary neutrophils fromperipheralblood	blood

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