Variant report

Variant	rs17135606
Chromosome Location	chr7:101183527-101183528
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101183466..101188316-chr7:101456098..101460720,6	MCF-7	breast:
2	chr7:101175649..101178492-chr7:101181142..101183684,2	K562	blood:
3	chr7:101169835..101171791-chr7:101181175..101183653,2	K562	blood:
4	chr7:101183184..101184839-chr7:101190313..101192262,2	K562	blood:
5	chr7:101175649..101178492-chr7:101180631..101183684,3	K562	blood:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs6969571	0.85[AMR][1000 genomes]
rs6969576	0.85[AMR][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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1030604	chr7:100717732-101223465	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
3	nsv888821	chr7:101091470-101311540	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv831078	chr7:101094945-101257486	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv888822	chr7:101105017-101330734	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv888824	chr7:101109073-101330734	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	esv1796652	chr7:101156017-101219459	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv888825	chr7:101168283-101330734	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101159600-101188200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr7:101160400-101186000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:101160600-101190400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:101161800-101186000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:101167200-101184200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:101170000-101183800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:101171800-101187800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:101176400-101190800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:101178400-101185800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:101179000-101186000	Weak transcription	Right Ventricle	heart
11	chr7:101179000-101188400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:101179200-101195000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:101181200-101186000	Weak transcription	A549	lung
14	chr7:101181400-101194000	Weak transcription	Spleen	Spleen
15	chr7:101181600-101194000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:101182200-101188400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:101182400-101186200	Weak transcription	Fetal Intestine Small	intestine
18	chr7:101182600-101185800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr7:101182600-101186000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr7:101182600-101186000	Weak transcription	Fetal Muscle Leg	muscle
21	chr7:101182600-101194000	Weak transcription	HepG2	liver
22	chr7:101183000-101185800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:101183000-101194000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:101183200-101190600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:101183400-101185800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:101183400-101185800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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