Variant report

Variant	rs231396
Chromosome Location	chr4:2833966-2833967
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:2831848..2834358-chr4:2936694..2939327,2	MCF-7	breast:
2	chr4:2824960..2827685-chr4:2829062..2834190,6	MCF-7	breast:
3	chr4:2832537..2834514-chr4:2839076..2842016,2	K562	blood:
4	chr4:2827397..2830522-chr4:2833485..2837299,4	MCF-7	breast:
5	chr4:2825882..2828322-chr4:2831549..2834473,2	K562	blood:
6	chr4:2831876..2837098-chr4:2843967..2847104,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000087266	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000087274	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1626813	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs189139	0.88[AFR][1000 genomes]
rs231339	0.80[AFR][1000 genomes]
rs231402	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv470002	chr4:2701098-2836628	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv516797	chr4:2723531-2836628	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv878448	chr4:2723531-2846799	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
7	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv1010533	chr4:2792848-2873441	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv461162	chr4:2794320-2846799	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv593436	chr4:2794320-2846799	Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2820600-2839000	Weak transcription	Right Atrium	heart
2	chr4:2820600-2839200	Weak transcription	Brain Angular Gyrus	brain
3	chr4:2820600-2844600	Weak transcription	Psoas Muscle	Psoas
4	chr4:2820800-2835200	Weak transcription	HUVEC	blood vessel
5	chr4:2820800-2835400	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:2820800-2839600	Weak transcription	NHEK	skin
7	chr4:2821000-2844400	Weak transcription	HMEC	breast
8	chr4:2821200-2834200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr4:2821200-2835400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:2821400-2836200	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr4:2821400-2837800	Weak transcription	Small Intestine	intestine
12	chr4:2821600-2835400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:2821800-2835800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr4:2821800-2835800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:2821800-2838000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:2821800-2838000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr4:2821800-2838200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:2821800-2838600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:2821800-2838800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:2821800-2844200	Weak transcription	Hela-S3	cervix
21	chr4:2822000-2835200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr4:2822000-2835600	Strong transcription	Colonic Mucosa	Colon
23	chr4:2822000-2836000	Strong transcription	Primary T cells from cord blood	blood
24	chr4:2822000-2837200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:2822000-2837600	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:2822200-2836400	Strong transcription	Thymus	Thymus
27	chr4:2822200-2837600	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr4:2822400-2835800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr4:2822400-2838200	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr4:2822600-2835800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:2822600-2835800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr4:2822600-2835800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:2822600-2836200	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr4:2822600-2836600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr4:2822600-2836600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:2822600-2836800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:2822600-2836800	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:2822600-2838200	Strong transcription	H1 Cell Line	embryonic stem cell
39	chr4:2822600-2838400	Strong transcription	Lung	lung
40	chr4:2822800-2838000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:2823200-2835000	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr4:2823800-2837000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr4:2823800-2837200	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:2823800-2837400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:2824000-2837200	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr4:2824200-2836400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:2824200-2838000	Strong transcription	Esophagus	oesophagus
48	chr4:2824200-2838200	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr4:2824200-2838200	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr4:2824400-2838400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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