Variant report

Variant	rs7821135
Chromosome Location	chr8:59805717-59805718
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:59801933..59804319-chr8:59804381..59806631,2	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16924330	1.00[AMR][1000 genomes]
rs16924339	1.00[AMR][1000 genomes]
rs16924342	1.00[AMR][1000 genomes]
rs16924384	1.00[AMR][1000 genomes]
rs7826909	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890938	chr8:59355053-59809785	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv890940	chr8:59785412-59809785	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv526468	chr8:59799820-59813809	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59764200-59806400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:59771400-59811000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr8:59773400-59808200	Weak transcription	Thymus	Thymus
4	chr8:59790800-59811200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr8:59791400-59811000	Weak transcription	Brain Angular Gyrus	brain
6	chr8:59794200-59820000	Weak transcription	Fetal Intestine Large	intestine
7	chr8:59794800-59811000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr8:59800600-59809800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr8:59800800-59809600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:59800800-59810600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:59800800-59811000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr8:59801000-59808000	Weak transcription	Dnd41	blood
13	chr8:59801400-59811000	Weak transcription	Primary T cells from cord blood	blood
14	chr8:59802200-59810800	Weak transcription	HUVEC	blood vessel
15	chr8:59802800-59826600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:59804200-59811000	Weak transcription	Gastric	stomach
17	chr8:59804400-59806000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr8:59804600-59806000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:59804600-59806600	Strong transcription	Fetal Thymus	thymus
20	chr8:59804800-59806200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr8:59805000-59812200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr8:59805000-59815200	Weak transcription	Fetal Heart	heart
23	chr8:59805200-59815600	Weak transcription	Fetal Stomach	stomach
24	chr8:59805400-59808000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:59805400-59808200	Weak transcription	Osteobl	bone
26	chr8:59805400-59808400	Weak transcription	Fetal Brain Male	brain
27	chr8:59805400-59810600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr8:59805400-59826800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr8:59805600-59805800	Enhancers	Colon Smooth Muscle	Colon
30	chr8:59805600-59811000	Weak transcription	NHDF-Ad	bronchial

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