Variant report

Variant	rs10305522
Chromosome Location	chr6:39055516-39055517
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:39054886..39057587-chr6:39057914..39060553,2	MCF-7	breast:
2	chr6:39055500..39058719-chr6:39195179..39198658,3	K562	blood:
3	chr6:38940723..38941491-chr6:39055376..39056317,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164626	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs12194951	1.00[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028088	chr6:38821047-39163549	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv538205	chr6:38821047-39163549	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv528286	chr6:39019503-39060478	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1031922	chr6:39034484-39060762	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv462919	chr6:39050384-39062990	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv602963	chr6:39050384-39062990	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10305522	SRF	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39021200-39072000	Weak transcription	Gastric	stomach
2	chr6:39024200-39057800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:39027400-39073000	Weak transcription	Pancreas	Pancrea
4	chr6:39043400-39082000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:39050400-39055600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:39052200-39055800	Weak transcription	Colon Smooth Muscle	Colon
7	chr6:39052600-39056200	Enhancers	Stomach Smooth Muscle	stomach
8	chr6:39052600-39060400	Enhancers	Fetal Heart	heart
9	chr6:39052800-39056000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr6:39053000-39072400	Weak transcription	Brain Germinal Matrix	brain
11	chr6:39053400-39055600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:39053400-39057200	Weak transcription	Lung	lung
13	chr6:39053400-39059600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr6:39053800-39058400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr6:39053800-39058600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr6:39054000-39057800	Enhancers	Psoas Muscle	Psoas
17	chr6:39054200-39056600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:39054200-39057800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:39054400-39056600	Weak transcription	Right Atrium	heart
20	chr6:39054800-39056600	Weak transcription	Left Ventricle	heart
21	chr6:39054800-39057600	Enhancers	Fetal Muscle Leg	muscle
22	chr6:39055000-39056400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr6:39055000-39056600	Weak transcription	Right Ventricle	heart
24	chr6:39055200-39055800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr6:39055200-39056000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:39055200-39056800	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr6:39055200-39057400	Enhancers	Fetal Lung	lung
28	chr6:39055200-39069800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:39055400-39057000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
30	chr6:39055400-39057400	Enhancers	Fetal Stomach	stomach

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