Variant report

Variant	rs322330
Chromosome Location	chr7:137012410-137012411
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1612615	1.00[AFR][1000 genomes]
rs1647174	1.00[AFR][1000 genomes]
rs1647178	1.00[AFR][1000 genomes]
rs1647180	1.00[AFR][1000 genomes]
rs1669028	1.00[AFR][1000 genomes]
rs1731949	1.00[AFR][1000 genomes]
rs320718	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv889240	chr7:136972027-137038092	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv889241	chr7:136976713-137038092	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv889242	chr7:137005808-137081223	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136991600-137013000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:136998200-137013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:137001800-137016200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:137002000-137013000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:137002000-137020000	Weak transcription	Fetal Stomach	stomach
6	chr7:137004800-137016200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:137008000-137013000	Weak transcription	NH-A	brain
8	chr7:137009400-137014600	Enhancers	Brain Substantia Nigra	brain
9	chr7:137010000-137014200	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:137010400-137014400	Enhancers	Brain Angular Gyrus	brain
11	chr7:137010400-137018200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
12	chr7:137010600-137016000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:137010600-137016200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr7:137010800-137016400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:137011000-137012600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:137011000-137013000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr7:137011000-137013200	Weak transcription	Esophagus	oesophagus
18	chr7:137011000-137016400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:137011000-137020800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:137011200-137013000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr7:137011200-137013200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:137011200-137016200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr7:137011800-137013000	Weak transcription	Fetal Muscle Leg	muscle
24	chr7:137012000-137012600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:137012000-137022600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr7:137012200-137012800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr7:137012200-137014000	Enhancers	Brain Hippocampus Middle	brain
28	chr7:137012400-137014200	Enhancers	HMEC	breast
29	chr7:137012400-137014400	Enhancers	Brain Anterior Caudate	brain
30	chr7:137012400-137016600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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