Variant report

Variant	rs16991605
Chromosome Location	chr22:33345777-33345778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr22:33345619-33345958	HepG2	liver:	n/a	n/a
2	TEAD4	chr22:33345630-33346110	HepG2	liver:	n/a	n/a
3	FOXA2	chr22:33345692-33346011	HepG2	liver:	n/a	n/a
4	FOXA1	chr22:33345668-33346013	HepG2	liver:	n/a	n/a
5	HDAC2	chr22:33345749-33346024	HepG2	liver:	n/a	n/a
6	GATA3	chr22:33345706-33346201	SK-N-SH	brain:	n/a	n/a
7	FOXA1	chr22:33345674-33346004	HepG2	liver:	n/a	n/a
8	CEBPB	chr22:33345763-33346057	HepG2	liver:	n/a	n/a
9	FOXA1	chr22:33345667-33346054	HepG2	liver:	n/a	n/a
10	ARID3A	chr22:33345728-33345803	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32846948-32860159..22:33339333-33353583	K562	blood:

Variant related genes	Relation type
SYN3	TF binding region
ENSG00000184459	Chromatin interaction

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

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

rs_ID	r²[population]
rs10222206	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10222305	0.83[AFR][1000 genomes]
rs11089596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11089597	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1119511	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1119512	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11912124	1.00[EUR][1000 genomes]
rs11914041	1.00[EUR][1000 genomes]
rs12373961	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1365835	0.81[AFR][1000 genomes]
rs1988647	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56076355	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56095662	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs695224	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7364251	1.00[EUR][1000 genomes]
rs7364286	1.00[EUR][1000 genomes]
rs8140502	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9619319	0.97[AFR][1000 genomes]
rs9619320	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9619322	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs9621606	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9621607	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9621608	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9621609	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621610	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9621613	0.92[YRI][hapmap]
rs9621614	0.91[YRI][hapmap];1.00[EUR][1000 genomes]
rs9621615	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[EUR][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	nsv531568	chr22:33336868-33480272	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33314000-33380800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr22:33340200-33346000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr22:33341600-33349600	Weak transcription	Fetal Brain Male	brain
4	chr22:33343000-33347000	Enhancers	Fetal Intestine Small	intestine
5	chr22:33343200-33345800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr22:33343200-33347400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr22:33343200-33372600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr22:33343600-33346800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr22:33343600-33353000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr22:33344200-33346400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr22:33344200-33360400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr22:33344400-33345800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr22:33344800-33346600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr22:33345000-33349200	Enhancers	Fetal Heart	heart
15	chr22:33345000-33350800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr22:33345200-33348200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr22:33345200-33348400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr22:33345400-33346000	Enhancers	HMEC	breast
19	chr22:33345400-33346200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr22:33345400-33346200	Enhancers	Lung	lung
21	chr22:33345400-33346200	Enhancers	Ovary	ovary
22	chr22:33345400-33346600	Enhancers	Pancreas	Pancrea
23	chr22:33345400-33347400	Enhancers	Fetal Intestine Large	intestine
24	chr22:33345400-33348400	Enhancers	Fetal Muscle Leg	muscle
25	chr22:33345400-33348600	Enhancers	Placenta	Placenta
26	chr22:33345400-33348600	Enhancers	Left Ventricle	heart
27	chr22:33345600-33346000	Enhancers	Stomach Smooth Muscle	stomach
28	chr22:33345600-33346600	Enhancers	Fetal Kidney	kidney
29	chr22:33345600-33346800	Enhancers	HepG2	liver
30	chr22:33345600-33346800	Enhancers	K562	blood
31	chr22:33345600-33348400	Enhancers	Fetal Lung	lung
32	chr22:33345600-33348600	Enhancers	Right Atrium	heart

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