Variant report

Variant	rs60802901
Chromosome Location	chr13:95831386-95831387
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	chr13:95827296..95830102-chr13:95830426..95833781,3	K562	blood:

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11839908	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4148489	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][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	nsv533659	chr13:95757713-96042149	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv832689	chr13:95759073-95921308	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3414638	chr13:95829338-95836932	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3348199	chr13:95829360-95837030	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3365191	chr13:95829757-95837316	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95752200-95844200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr13:95778800-95833400	Weak transcription	Spleen	Spleen
3	chr13:95799200-95833400	Weak transcription	HSMMtube	muscle
4	chr13:95807000-95846000	Weak transcription	Brain Substantia Nigra	brain
5	chr13:95807000-95857800	Weak transcription	Esophagus	oesophagus
6	chr13:95807200-95844400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr13:95807200-95865600	Weak transcription	Colonic Mucosa	Colon
8	chr13:95807400-95837800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr13:95808200-95841800	Weak transcription	Osteobl	bone
10	chr13:95808400-95833400	Weak transcription	Fetal Kidney	kidney
11	chr13:95808400-95854600	Weak transcription	NHEK	skin
12	chr13:95810400-95836200	Weak transcription	Fetal Thymus	thymus
13	chr13:95810400-95836400	Weak transcription	Thymus	Thymus
14	chr13:95812400-95831400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr13:95812800-95833400	Weak transcription	Pancreas	Pancrea
16	chr13:95813200-95858000	Weak transcription	Aorta	Aorta
17	chr13:95814600-95832400	Weak transcription	HepG2	liver
18	chr13:95814800-95833400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr13:95815000-95844200	Weak transcription	Fetal Muscle Leg	muscle
20	chr13:95815200-95847800	Weak transcription	Hela-S3	cervix
21	chr13:95817200-95833400	Weak transcription	Psoas Muscle	Psoas
22	chr13:95817400-95832800	Weak transcription	Stomach Mucosa	stomach
23	chr13:95818200-95841800	Weak transcription	NHDF-Ad	bronchial
24	chr13:95822000-95834600	Weak transcription	Fetal Stomach	stomach
25	chr13:95822000-95837000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr13:95823600-95844400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr13:95824400-95833400	Weak transcription	Left Ventricle	heart
28	chr13:95824600-95840000	Weak transcription	Fetal Lung	lung
29	chr13:95824800-95831400	Strong transcription	A549	lung
30	chr13:95825400-95841400	Weak transcription	HUVEC	blood vessel
31	chr13:95826000-95833800	Weak transcription	K562	blood
32	chr13:95826800-95831400	Strong transcription	NHLF	lung
33	chr13:95827200-95838000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:95827400-95832000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr13:95827400-95832000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr13:95827400-95833000	Weak transcription	Colon Smooth Muscle	Colon
37	chr13:95827400-95833400	Weak transcription	Gastric	stomach
38	chr13:95827400-95872400	Weak transcription	NH-A	brain
39	chr13:95827800-95832000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:95828000-95840400	Weak transcription	Liver	Liver
41	chr13:95828400-95832800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr13:95828600-95833800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr13:95828600-95844200	Weak transcription	HSMM	muscle
44	chr13:95829000-95831400	Strong transcription	GM12878-XiMat	blood
45	chr13:95829000-95831600	Strong transcription	Fetal Intestine Large	intestine
46	chr13:95829000-95831600	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr13:95829400-95833000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr13:95829400-95840400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr13:95829400-95856000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr13:95829600-95834400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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