Variant report

Variant	rs17143822
Chromosome Location	chr7:21115660-21115661
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs6946835	0.91[AFR][1000 genomes]

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	nsv830920	chr7:21014535-21201580	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv3478244	chr7:21044211-21417347	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3478245	chr7:21044211-21417347	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1020852	chr7:21060791-21375050	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv538799	chr7:21060791-21375050	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21111000-21120600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:21111800-21115800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:21114800-21117000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:21115000-21116000	Enhancers	Fetal Lung	lung
5	chr7:21115000-21116200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr7:21115000-21117000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:21115200-21116000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:21115200-21116400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr7:21115200-21117000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:21115200-21117000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:21115200-21117400	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr7:21115400-21116600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:21115400-21116800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:21115400-21117400	Enhancers	Fetal Kidney	kidney
15	chr7:21115600-21116400	Enhancers	Fetal Intestine Large	intestine
16	chr7:21115600-21116800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:21115600-21117000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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