Variant report

Variant	rs35401074
Chromosome Location	chr9:137003821-137003822
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:137003273-137004552	HepG2	liver:	n/a	n/a
2	POLR2A	chr9:137003817-137003909	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr9:137003027-137004048	K562	blood:	n/a	n/a
4	CTCF	chr9:137003820-137003970	HEEpiC	esophagus:	n/a	n/a
5	POLR2A	chr9:137003617-137004304	MCF10A-Er-Src	breast:	n/a	n/a
6	CTCF	chr9:137003780-137003930	Caco-2	colon:	n/a	n/a
7	POLR2A	chr9:137003222-137003999	SK-N-MC	brain:	n/a	n/a
8	POLR2A	chr9:137003809-137004021	HepG2	liver:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:137001564..137003951-chr9:137325246..137326831,2	MCF-7	breast:
2	chr9:136932690..136935080-chr9:137003441..137005032,2	MCF-7	breast:
3	chr9:136928987..136935981-chr9:136998799..137005312,16	MCF-7	breast:
4	chr9:137003283..137007180-chr9:137027026..137030232,3	K562	blood:

No data

Variant related genes	Relation type
WDR5	TF binding region
ENSG00000273249	TF binding region
ENSG00000169925	Chromatin interaction
ENSG00000221676	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1128044	0.83[ASN][1000 genomes]
rs11556390	0.86[ASN][1000 genomes]
rs28412218	0.82[ASN][1000 genomes]
rs28415637	0.85[ASN][1000 genomes]
rs28428662	0.83[ASN][1000 genomes]
rs28438574	0.85[ASN][1000 genomes]
rs28475221	0.87[ASN][1000 genomes]
rs28485659	0.84[ASN][1000 genomes]
rs28490920	0.86[ASN][1000 genomes]
rs28508246	0.86[ASN][1000 genomes]
rs28522840	0.85[ASN][1000 genomes]
rs28549758	0.86[ASN][1000 genomes]
rs28567437	0.85[ASN][1000 genomes]
rs28588875	0.86[ASN][1000 genomes]
rs28604373	0.84[ASN][1000 genomes]
rs28610236	0.85[ASN][1000 genomes]
rs28611335	0.83[ASN][1000 genomes]
rs28635910	0.84[ASN][1000 genomes]
rs28637447	0.84[ASN][1000 genomes]
rs28647893	0.82[ASN][1000 genomes]
rs28648812	0.85[ASN][1000 genomes]
rs28661406	0.84[ASN][1000 genomes]
rs28681320	0.84[ASN][1000 genomes]
rs28695913	0.86[ASN][1000 genomes]
rs28705801	0.85[ASN][1000 genomes]
rs34417824	0.86[ASN][1000 genomes]
rs35715743	0.86[ASN][1000 genomes]
rs35949820	0.85[ASN][1000 genomes]
rs36185416	0.82[ASN][1000 genomes]
rs55874211	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894138	chr9:136839840-137093168	Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv825148	chr9:136848471-137025632	Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1048571	chr9:136872166-137265444	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv894148	chr9:136874066-137093168	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv894151	chr9:136887757-137397609	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
6	nsv6751	chr9:136967475-137007131	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv894155	chr9:136969689-137364866	Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
8	esv1793302	chr9:136990615-137390602	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:137001600-137004600	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr9:137001800-137004400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:137002000-137004800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:137002200-137004200	Enhancers	Fetal Heart	heart
5	chr9:137002200-137004400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr9:137002400-137004000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr9:137002400-137004200	Enhancers	Gastric	stomach
8	chr9:137002400-137004200	Enhancers	Lung	lung
9	chr9:137002400-137004400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:137002400-137004400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr9:137002400-137004400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr9:137002400-137004400	Enhancers	Small Intestine	intestine
13	chr9:137002400-137004600	Enhancers	Primary T cells fromperipheralblood	blood
14	chr9:137002400-137004600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr9:137002400-137004600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr9:137002400-137004600	Enhancers	Esophagus	oesophagus
17	chr9:137002400-137004600	Enhancers	Ovary	ovary
18	chr9:137002400-137004600	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr9:137002400-137004800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr9:137002400-137004800	Enhancers	Adipose Nuclei	Adipose
21	chr9:137002400-137004800	Enhancers	Left Ventricle	heart
22	chr9:137002400-137005600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr9:137002400-137006400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:137002400-137016200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr9:137002600-137004000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr9:137002600-137004000	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr9:137002600-137004000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr9:137002600-137004000	Weak transcription	HUVEC	blood vessel
29	chr9:137002600-137004200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:137002600-137004200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr9:137002600-137004200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr9:137002600-137004200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr9:137002600-137004400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr9:137002600-137004400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:137002600-137004400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr9:137002600-137004400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:137002600-137004400	Enhancers	Right Ventricle	heart
38	chr9:137002600-137004600	Enhancers	Brain Substantia Nigra	brain
39	chr9:137002600-137004800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr9:137002600-137005000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr9:137002600-137005000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr9:137002600-137005000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr9:137002600-137005000	Enhancers	Pancreas	Pancrea
44	chr9:137002600-137005200	Genic enhancers	Fetal Intestine Small	intestine
45	chr9:137002600-137005800	Genic enhancers	Fetal Stomach	stomach
46	chr9:137002800-137004000	Genic enhancers	A549	lung
47	chr9:137002800-137004200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr9:137002800-137004600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr9:137002800-137004800	Enhancers	Colon Smooth Muscle	Colon
50	chr9:137003000-137004200	Genic enhancers	iPS-20b Cell Line	embryonic stem cell

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