Variant report

Variant	rs7758814
Chromosome Location	chr6:149276464-149276465
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:149067550..149069400-chr6:149273636..149276626,2	MCF-7	breast:
2	chr6:148899066..148899621-chr6:149276241..149276823,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZC3H12D-3	chr6:149275397-149277289	NONHSAT115482

Variant related genes	Relation type
ENSG00000111962	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs17079591	1.00[EUR][1000 genomes]
rs34564476	1.00[AFR][1000 genomes]
rs6921380	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7752857	1.00[EUR][1000 genomes]
rs7765192	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv830842	chr6:149272321-149427340	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149256600-149292600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:149257000-149285000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr6:149261400-149285000	Weak transcription	Spleen	Spleen
4	chr6:149262000-149289600	Weak transcription	Aorta	Aorta
5	chr6:149269200-149276600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:149269400-149277600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:149269400-149288800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:149269400-149291400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:149269600-149277800	Weak transcription	Brain Substantia Nigra	brain
10	chr6:149271200-149276600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:149271200-149288600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:149271600-149277600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr6:149271600-149285600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:149272800-149283400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:149274000-149277200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:149274000-149286400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:149274000-149288800	Weak transcription	NHEK	skin
18	chr6:149274000-149293800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:149274200-149276600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:149274200-149284000	Weak transcription	Ovary	ovary
21	chr6:149274200-149288400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr6:149274200-149288800	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:149274400-149290400	Weak transcription	Fetal Kidney	kidney
24	chr6:149274600-149288600	Weak transcription	Colon Smooth Muscle	Colon
25	chr6:149274600-149289000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:149275400-149278000	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr6:149275400-149278200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:149275600-149276800	Enhancers	Duodenum Mucosa	Duodenum
29	chr6:149275600-149276800	Enhancers	Fetal Lung	lung
30	chr6:149275600-149277200	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr6:149275600-149277200	Enhancers	Fetal Heart	heart
32	chr6:149275600-149277400	Strong transcription	H9 Cell Line	embryonic stem cell
33	chr6:149275600-149277600	Strong transcription	Primary B cells from cord blood	blood
34	chr6:149275600-149277800	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:149275600-149277800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:149275600-149278000	Strong transcription	Primary B cells from peripheral blood	blood
37	chr6:149275800-149276800	Enhancers	Fetal Intestine Small	intestine
38	chr6:149275800-149277000	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr6:149275800-149277000	Enhancers	Brain Germinal Matrix	brain
40	chr6:149275800-149278400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:149276000-149276600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:149276000-149276600	Enhancers	Fetal Intestine Large	intestine
43	chr6:149276000-149276800	Genic enhancers	Fetal Stomach	stomach
44	chr6:149276000-149277000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:149276000-149277200	Enhancers	Placenta	Placenta
46	chr6:149276000-149278000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr6:149276000-149278200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr6:149276200-149276600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:149276200-149276600	Enhancers	Pancreas	Pancrea
50	chr6:149276200-149276800	Enhancers	Fetal Muscle Leg	muscle

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