Variant report

Variant	rs7774073
Chromosome Location	chr6:37049768-37049769
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:37028754..37030470-chr6:37049218..37051479,2	K562	blood:
2	chr6:37035293..37037113-chr6:37048095..37050950,2	K562	blood:
3	chr6:37045453..37048349-chr6:37049676..37051329,3	K562	blood:
4	chr6:37047930..37050667-chr6:37174268..37176319,2	K562	blood:
5	chr6:37045369..37048087-chr6:37049023..37051325,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10223714	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12216069	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2094575	0.86[ASN][1000 genomes]
rs2149336	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4711483	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4714035	0.85[EUR][1000 genomes]
rs6457976	0.85[ASN][1000 genomes]
rs6457978	0.90[ASN][1000 genomes]
rs6457979	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6457980	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6917684	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6924660	0.86[ASN][1000 genomes]
rs7748291	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7750403	0.88[ASN][1000 genomes]
rs7750614	0.86[ASN][1000 genomes]
rs7750717	0.86[ASN][1000 genomes]
rs7751821	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7770544	0.86[ASN][1000 genomes]
rs913499	0.88[ASN][1000 genomes]
rs913500	0.80[ASN][1000 genomes]
rs9296208	0.86[ASN][1000 genomes]
rs9366927	0.85[ASN][1000 genomes]
rs9380638	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9394401	0.88[ASN][1000 genomes]
rs9394402	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9394403	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9462258	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9470469	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37040000-37051200	Weak transcription	A549	lung
2	chr6:37045800-37050600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:37045800-37051000	Weak transcription	Colonic Mucosa	Colon
4	chr6:37045800-37051000	Weak transcription	Left Ventricle	heart
5	chr6:37045800-37051000	Weak transcription	Lung	lung
6	chr6:37045800-37051000	Weak transcription	Right Atrium	heart
7	chr6:37045800-37051400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:37045800-37060800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:37046000-37051000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:37046000-37051000	Weak transcription	Esophagus	oesophagus
11	chr6:37046000-37051000	Weak transcription	Right Ventricle	heart
12	chr6:37046000-37051200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:37046200-37051000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:37046200-37051000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:37046200-37051000	Weak transcription	NHEK	skin
16	chr6:37046400-37050400	Weak transcription	Placenta	Placenta
17	chr6:37046400-37050600	Weak transcription	Ovary	ovary
18	chr6:37046400-37050600	Weak transcription	HMEC	breast
19	chr6:37046400-37051000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:37046400-37051000	Weak transcription	Fetal Lung	lung
21	chr6:37046600-37051000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:37046800-37050600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:37046800-37050800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr6:37046800-37051200	Weak transcription	Colon Smooth Muscle	Colon
25	chr6:37047000-37049800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:37047000-37051000	Weak transcription	Fetal Stomach	stomach
27	chr6:37047000-37051000	Weak transcription	Osteobl	bone
28	chr6:37047000-37051200	Weak transcription	NHLF	lung
29	chr6:37047200-37051200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:37047600-37050800	Enhancers	HepG2	liver
31	chr6:37047600-37051000	Weak transcription	NHDF-Ad	bronchial
32	chr6:37047800-37050600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:37048000-37050400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr6:37048400-37050200	Weak transcription	Spleen	Spleen
35	chr6:37048800-37052600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr6:37049000-37051000	Enhancers	K562	blood
37	chr6:37049200-37050400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr6:37049200-37051000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr6:37049600-37050600	Enhancers	Liver	Liver
40	chr6:37049600-37052200	Enhancers	Adipose Nuclei	Adipose
41	chr6:37049600-37052800	Enhancers	Fetal Intestine Large	intestine
42	chr6:37049600-37053200	Enhancers	Fetal Intestine Small	intestine

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