Variant report

Variant	rs10138768
Chromosome Location	chr14:104190527-104190528
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:104190500-104190650	AoAF	blood vessel:	n/a	chr14:104190590-104190603
2	CTCF	chr14:104190500-104190650	HPAF	blood vessel:	n/a	chr14:104190590-104190603
3	CTCF	chr14:104190520-104190670	HRPEpiC	eye:	n/a	chr14:104190590-104190603
4	CTCF	chr14:104190480-104190630	HA-sp	spinal cord:	n/a	chr14:104190590-104190603
5	CTCF	chr14:104190500-104190650	NHEK	skin:	n/a	chr14:104190590-104190603
6	RAD21	chr14:104190404-104190703	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr14:104190520-104190670	HMF	breast:	n/a	chr14:104190590-104190603
8	GATA1	chr14:104190349-104191203	PBDE	blood:	n/a	chr14:104190763-104190770 chr14:104190763-104190770 chr14:104190763-104190770
9	CTCF	chr14:104190480-104190630	HRPEpiC	eye:	n/a	chr14:104190590-104190603
10	CTCF	chr14:104190500-104190650	HRE	kidney:	n/a	chr14:104190590-104190603
11	HMGN3	chr14:104190405-104190541	K562	blood:	n/a	n/a
12	CTCF	chr14:104190520-104190670	HCPEpiC	choroid plexus:	n/a	chr14:104190590-104190603
13	CTCF	chr14:104190500-104190650	HCM	heart:	n/a	chr14:104190590-104190603

No.	Distal block	Cell Line	Cell type
1	chr14:104190172..104192468-chr14:104312606..104314249,2	MCF-7	breast:
2	chr14:104189773..104192879-chr14:104194164..104195962,3	K562	blood:
3	chr14:104178608..104186342-chr14:104186894..104193138,16	K562	blood:
4	chr14:104188793..104191083-chr14:104192402..104194105,2	MCF-7	breast:

Variant related genes	Relation type
ZFYVE21	TF binding region
ENSG00000088808	Chromatin interaction
ENSG00000258735	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000269963	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs3212124	1.00[YRI][hapmap]
rs8548	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	162 gene(s)	inside rSNPs	diseases
2	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
3	nsv1052010	chr14:104061472-104216267	Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv542201	chr14:104061472-104216267	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv456435	chr14:104061646-104198251	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv566023	chr14:104061646-104198251	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
7	nsv902308	chr14:104087209-104211180	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv1041329	chr14:104097750-104196346	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv542202	chr14:104097750-104196346	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv1048866	chr14:104100862-104195896	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
12	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
13	nsv902309	chr14:104143385-104198251	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv902310	chr14:104143385-104205811	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
16	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
17	nsv902311	chr14:104148339-104205811	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
18	nsv902312	chr14:104155317-104211180	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
19	nsv527425	chr14:104162263-104198251	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
20	nsv470673	chr14:104162263-104219949	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
21	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
22	nsv902315	chr14:104165927-104190527	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
23	nsv902316	chr14:104173823-104195161	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv902317	chr14:104175676-104194278	Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104183200-104191800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr14:104183400-104192400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:104183400-104195000	Weak transcription	Primary B cells from cord blood	blood
4	chr14:104183400-104200600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr14:104183600-104192200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr14:104183600-104192400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr14:104183600-104192600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:104183600-104194200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr14:104183600-104194200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr14:104183600-104194200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr14:104183600-104194800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:104183600-104195000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr14:104183600-104195200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr14:104183800-104194000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr14:104183800-104194200	Strong transcription	Fetal Intestine Small	intestine
16	chr14:104183800-104194600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr14:104183800-104195200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr14:104183800-104195400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:104184000-104191200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr14:104184000-104192200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:104184000-104195400	Weak transcription	Fetal Kidney	kidney
22	chr14:104184000-104201200	Weak transcription	HUVEC	blood vessel
23	chr14:104184000-104209000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr14:104184200-104214400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr14:104184400-104211000	Weak transcription	Hela-S3	cervix
26	chr14:104184600-104192600	Enhancers	Fetal Muscle Trunk	muscle
27	chr14:104185000-104190600	Weak transcription	Dnd41	blood
28	chr14:104185200-104191400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:104185200-104194800	Weak transcription	GM12878-XiMat	blood
30	chr14:104185400-104190600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:104185400-104191000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:104185400-104192200	Weak transcription	HepG2	liver
33	chr14:104185400-104194200	Weak transcription	NHDF-Ad	bronchial
34	chr14:104185600-104194600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr14:104186200-104195200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr14:104186400-104192000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr14:104186400-104192400	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr14:104186400-104194200	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr14:104186600-104192800	Weak transcription	Primary T cells from cord blood	blood
40	chr14:104186800-104195800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr14:104187000-104190800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr14:104187200-104190600	Enhancers	Esophagus	oesophagus
43	chr14:104187600-104192000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:104187800-104190600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:104187800-104191600	Enhancers	HSMM	muscle
46	chr14:104188000-104194000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr14:104188200-104191200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr14:104188200-104195000	Weak transcription	A549	lung
49	chr14:104188400-104190600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:104188400-104190600	Weak transcription	Thymus	Thymus

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