Variant report

Variant	rs35472599
Chromosome Location	chr7:104573738-104573739
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:104573476..104576599-chr7:104652408..104655277,3	MCF-7	breast:
2	chr7:104571186..104579198-chr7:104651179..104656823,10	K562	blood:
3	chr7:104572713..104579198-chr7:104651179..104657046,8	K562	blood:
4	chr7:104571846..104574043-chr7:104575811..104577393,2	K562	blood:

Variant related genes	Relation type
ENSG00000228393	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000239569	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10274325	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12668896	0.83[AMR][1000 genomes]
rs13239438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2073972	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35110258	0.94[ASN][1000 genomes]
rs60137855	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs61192398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9791783	0.84[AMR][1000 genomes];0.95[ASN][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	nsv831086	chr7:104422503-104596766	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv3421532	chr7:104571416-104575714	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1029283	chr7:104571741-104729168	Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	132 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104564000-104574600	Weak transcription	HSMM	muscle
2	chr7:104567200-104575200	Enhancers	Fetal Intestine Small	intestine
3	chr7:104569800-104580600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:104569800-104584000	Weak transcription	Esophagus	oesophagus
5	chr7:104570200-104574400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:104570400-104575400	Enhancers	Primary B cells from peripheral blood	blood
7	chr7:104570600-104575400	Enhancers	Stomach Mucosa	stomach
8	chr7:104571400-104574200	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr7:104571400-104575200	Enhancers	Fetal Intestine Large	intestine
10	chr7:104572200-104574000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:104572200-104577000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:104572200-104580000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:104572200-104580800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:104572800-104573800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr7:104572800-104574400	Flanking Active TSS	Primary B cells from cord blood	blood
16	chr7:104572800-104579400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:104573400-104573800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
18	chr7:104573400-104573800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:104573400-104573800	ZNF genes & repeats	Fetal Kidney	kidney
20	chr7:104573400-104573800	Enhancers	Gastric	stomach
21	chr7:104573400-104573800	Enhancers	Pancreas	Pancrea
22	chr7:104573400-104573800	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr7:104573400-104574000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:104573400-104574000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:104573400-104574000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:104573400-104574000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:104573400-104574000	Enhancers	Brain Substantia Nigra	brain
28	chr7:104573400-104574000	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr7:104573400-104574000	ZNF genes & repeats	Fetal Brain Male	brain
30	chr7:104573400-104574000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr7:104573400-104574000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr7:104573400-104574000	Active TSS	Rectal Smooth Muscle	rectum
33	chr7:104573400-104574000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr7:104573400-104574200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:104573400-104574200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:104573400-104574200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:104573400-104574200	Enhancers	Spleen	Spleen
38	chr7:104573400-104574200	Enhancers	GM12878-XiMat	blood
39	chr7:104573400-104574600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr7:104573400-104580200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:104573600-104573800	Enhancers	Fetal Heart	heart
42	chr7:104573600-104573800	Bivalent/Poised TSS	Fetal Lung	lung
43	chr7:104573600-104574000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr7:104573600-104574000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:104573600-104574000	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr7:104573600-104574000	Flanking Active TSS	Colonic Mucosa	Colon
47	chr7:104573600-104574200	Enhancers	Small Intestine	intestine
48	chr7:104573600-104574200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:104573600-104574400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:104573600-104576800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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