Variant report

Variant	rs7503083
Chromosome Location	chr17:37901456-37901457
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:37773726..37775508-chr17:37899665..37902639,2	MCF-7	breast:
2	chr17:37895749..37897713-chr17:37900538..37902317,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000141738	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs12453736	1.00[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv1056234	chr17:37862605-37909988	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv908219	chr17:37880265-37917633	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv1064787	chr17:37892843-38054410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	nsv543342	chr17:37892843-38054410	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37897200-37909400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:37897800-37906400	Weak transcription	Right Ventricle	heart
3	chr17:37897800-37910000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr17:37898000-37905200	Strong transcription	Fetal Intestine Small	intestine
5	chr17:37898200-37903600	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr17:37898400-37904400	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr17:37898400-37906000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr17:37898600-37902400	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr17:37898600-37902800	Strong transcription	NHEK	skin
10	chr17:37898600-37903400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr17:37898600-37904000	Strong transcription	Liver	Liver
12	chr17:37898600-37904400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
13	chr17:37898600-37904400	Strong transcription	Fetal Intestine Large	intestine
14	chr17:37898800-37904200	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr17:37898800-37904400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr17:37899000-37902800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr17:37899000-37903000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr17:37899000-37903200	Strong transcription	HMEC	breast
19	chr17:37899000-37903400	Strong transcription	Colonic Mucosa	Colon
20	chr17:37899000-37903800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr17:37899000-37904000	Strong transcription	Placenta Amnion	Placenta Amnion
22	chr17:37899000-37904200	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr17:37899000-37904400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr17:37899000-37904400	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr17:37899200-37902200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr17:37899200-37904200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr17:37899400-37904000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr17:37899400-37904200	Strong transcription	Esophagus	oesophagus
29	chr17:37899400-37904400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr17:37899400-37904400	Strong transcription	Gastric	stomach
31	chr17:37899400-37904800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr17:37899400-37906400	Weak transcription	Spleen	Spleen
33	chr17:37899600-37902200	Strong transcription	Lung	lung
34	chr17:37899600-37904400	Strong transcription	Pancreas	Pancrea
35	chr17:37899800-37904200	Strong transcription	HepG2	liver
36	chr17:37900000-37902200	Enhancers	HUVEC	blood vessel
37	chr17:37900400-37901600	Strong transcription	Fetal Kidney	kidney
38	chr17:37900400-37901600	Strong transcription	A549	lung
39	chr17:37900600-37902200	Strong transcription	Pancreatic Islets	Pancreatic Islet
40	chr17:37900600-37903400	Strong transcription	Sigmoid Colon	Sigmoid Colon
41	chr17:37901000-37904400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr17:37901200-37903400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr17:37901200-37903800	Strong transcription	Placenta	Placenta
44	chr17:37901200-37904200	Strong transcription	Fetal Stomach	stomach
45	chr17:37901200-37906200	Weak transcription	Stomach Mucosa	stomach
46	chr17:37901400-37902000	Weak transcription	Hela-S3	cervix
47	chr17:37901400-37906400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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