Variant report

Variant	rs185253371
Chromosome Location	chr7:104850861-104850862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:104842758..104847197-chr7:104847496..104851366,4	MCF-7	breast:
2	chr7:104845667..104848207-chr7:104850068..104852125,2	K562	blood:
3	chr7:104850289..104852047-chr7:104854189..104856772,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000271482	Chromatin interaction
ENSG00000135250	Chromatin interaction

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	esv34588	chr7:104737612-105153242	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv2757233	chr7:104758250-105208492	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	esv2759549	chr7:104758250-105208492	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats 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	39 gene(s)	inside rSNPs	diseases
4	nsv8196	chr7:104763559-105155978	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS 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	17 gene(s)	inside rSNPs	diseases
5	esv34580	chr7:104763580-105153242	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	esv2758127	chr7:104766707-105110581	Enhancers Strong transcription Active TSS Flanking Active TSS Weak 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	15 gene(s)	inside rSNPs	diseases
7	nsv1028228	chr7:104807207-105182998	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv932138	chr7:104826194-105152816	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv1015688	chr7:104849770-105182998	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv967467	chr7:104850694-104859017	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104822000-104858800	Weak transcription	Gastric	stomach
2	chr7:104828600-104851000	Weak transcription	Stomach Mucosa	stomach
3	chr7:104831200-104851000	Weak transcription	Pancreas	Pancrea
4	chr7:104834600-104851000	Weak transcription	Small Intestine	intestine
5	chr7:104839400-104858400	Weak transcription	NHLF	lung
6	chr7:104839600-104857200	Weak transcription	A549	lung
7	chr7:104841200-104853400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:104841600-104851200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:104842000-104851000	Weak transcription	Ovary	ovary
10	chr7:104842000-104851000	Weak transcription	HUVEC	blood vessel
11	chr7:104842200-104865400	Weak transcription	K562	blood
12	chr7:104842400-104857200	Weak transcription	HMEC	breast
13	chr7:104842800-104851200	Weak transcription	Esophagus	oesophagus
14	chr7:104843200-104863400	Weak transcription	HepG2	liver
15	chr7:104843600-104851200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr7:104843800-104851000	Weak transcription	Psoas Muscle	Psoas
17	chr7:104843800-104851000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr7:104843800-104851200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:104843800-104851200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:104843800-104851200	Weak transcription	Right Ventricle	heart
21	chr7:104843800-104851200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr7:104843800-104859600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:104844000-104863200	Weak transcription	Fetal Intestine Large	intestine
24	chr7:104844200-104851000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:104844200-104851000	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:104844200-104869000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr7:104844200-104869000	Weak transcription	Fetal Intestine Small	intestine
28	chr7:104844200-104869000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr7:104844400-104851200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:104844400-104851200	Weak transcription	Adipose Nuclei	Adipose
31	chr7:104844600-104857800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:104845200-104851800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr7:104845400-104851200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr7:104845400-104851200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:104845400-104857000	Weak transcription	NHEK	skin
36	chr7:104845400-104857200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:104845400-104858800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr7:104845600-104851200	Weak transcription	Lung	lung
39	chr7:104845600-104851800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:104846600-104851000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr7:104846600-104851200	Weak transcription	Left Ventricle	heart
42	chr7:104846600-104851200	Weak transcription	Spleen	Spleen
43	chr7:104846600-104852800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr7:104847000-104851000	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr7:104847200-104851400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:104847200-104862600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:104847800-104851000	Weak transcription	Right Atrium	heart
48	chr7:104848600-104854600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr7:104848600-104860200	Genic enhancers	Dnd41	blood
50	chr7:104849000-104851600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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