Variant report

Variant	rs35641096
Chromosome Location	chr7:136563373-136563374
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	chr7:136561220..136563776-chr7:136565469..136567978,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10488595	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10488596	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10488597	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10954565	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10954566	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11763464	1.00[ASN][1000 genomes]
rs11771119	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12530999	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12532627	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12532672	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12533282	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12534748	0.88[AMR][1000 genomes]
rs12536964	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12537069	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12537753	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12537831	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12538445	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12670040	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13222744	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223210	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13223738	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13230245	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13233131	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13233495	0.88[AMR][1000 genomes]
rs13235508	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13235822	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13243456	0.88[AMR][1000 genomes]
rs1424574	0.88[AMR][1000 genomes]
rs17409631	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17409769	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17487790	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17494540	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17494589	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34166421	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34617713	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34653588	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35310233	0.88[AMR][1000 genomes]
rs35784011	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36007709	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62485215	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62485218	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62485222	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62485223	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71541328	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71541330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[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	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

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136557000-136567800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:136558000-136609200	Weak transcription	Left Ventricle	heart
3	chr7:136560600-136564000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:136560600-136566800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:136561200-136569000	Enhancers	Fetal Heart	heart
6	chr7:136561400-136563400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr7:136561400-136565000	Enhancers	Rectal Smooth Muscle	rectum
8	chr7:136561800-136564800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:136562000-136563400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr7:136562200-136563400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:136562200-136565200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:136562400-136564000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:136562400-136565000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:136562600-136564400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:136562600-136565000	Enhancers	Colon Smooth Muscle	Colon
16	chr7:136562800-136564000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:136563000-136563400	Weak transcription	NHLF	lung
18	chr7:136563200-136564000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:136563200-136567000	Weak transcription	Stomach Smooth Muscle	stomach

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