Variant report

Variant	rs17102000
Chromosome Location	chr14:65182726-65182727
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:65182060..65184778-chr14:65193626..65195204,2	MCF-7	breast:
2	chr14:65182239..65187467-chr14:65224192..65227180,5	MCF-7	breast:
3	chr14:65182677..65185308-chr14:65185864..65187831,2	K562	blood:
4	chr14:65182089..65184579-chr17:56735427..56737883,2	MCF-7	breast:
5	chr14:65168529..65178400-chr14:65179583..65195815,52	MCF-7	breast:

Variant related genes	Relation type
ENSG00000070182	Chromatin interaction
ENSG00000126822	Chromatin interaction
ENSG00000202077	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10138311	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17101919	1.00[MEX][hapmap]
rs17102003	0.86[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17102005	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17102007	1.00[ASW][hapmap];0.83[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17102018	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs17102019	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs17102026	1.00[MEX][hapmap]
rs17102170	1.00[MEX][hapmap]
rs229577	1.00[MEX][hapmap]
rs229578	1.00[MEX][hapmap]
rs41456047	1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs4453374	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59115111	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73271697	1.00[ASN][1000 genomes]
rs74056388	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74056389	1.00[ASN][1000 genomes]
rs74056391	1.00[ASN][1000 genomes]
rs74056394	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74056396	0.85[AFR][1000 genomes];1.00[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	nsv1049097	chr14:65027753-65202018	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv1818582	chr14:65172898-65256685	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1035833	chr14:65176371-65246181	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65176000-65186400	Weak transcription	Osteobl	bone
2	chr14:65177000-65189200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:65177200-65183400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr14:65180800-65185400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:65181000-65189400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr14:65181000-65197600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr14:65181200-65183800	Weak transcription	Hela-S3	cervix
8	chr14:65181200-65184400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr14:65181200-65185800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:65181200-65189600	Enhancers	Liver	Liver
11	chr14:65181200-65197000	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr14:65181400-65183000	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr14:65181400-65183400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr14:65181400-65183600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr14:65181400-65184800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:65181600-65183400	Weak transcription	Lung	lung
17	chr14:65181600-65183600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr14:65181600-65189400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr14:65181800-65183200	Enhancers	Fetal Lung	lung
20	chr14:65181800-65183200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr14:65181800-65183400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:65181800-65184200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:65181800-65184600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:65181800-65185000	Enhancers	Fetal Muscle Trunk	muscle
25	chr14:65181800-65186200	Enhancers	Fetal Muscle Leg	muscle
26	chr14:65181800-65188800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr14:65181800-65190600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr14:65181800-65192400	Enhancers	Adipose Nuclei	Adipose
29	chr14:65181800-65194400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr14:65182000-65182800	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr14:65182000-65182800	Enhancers	HepG2	liver
32	chr14:65182000-65183000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
33	chr14:65182000-65183000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr14:65182000-65183400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:65182000-65183400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr14:65182000-65183400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr14:65182000-65183600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:65182000-65185200	Enhancers	Fetal Kidney	kidney
39	chr14:65182000-65185800	Enhancers	Gastric	stomach
40	chr14:65182000-65190800	Enhancers	Stomach Mucosa	stomach
41	chr14:65182200-65183000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr14:65182200-65183400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr14:65182200-65183400	Active TSS	Brain Anterior Caudate	brain
44	chr14:65182200-65183400	Enhancers	Fetal Brain Male	brain
45	chr14:65182200-65183800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr14:65182200-65183800	Flanking Active TSS	Pancreas	Pancrea
47	chr14:65182200-65184000	Flanking Active TSS	HMEC	breast
48	chr14:65182200-65184200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr14:65182200-65184400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr14:65182200-65184400	Enhancers	Skeletal Muscle Female	skeletal muscle

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